2074 lines
112 KiB
HTML
2074 lines
112 KiB
HTML
|
||
<!DOCTYPE html>
|
||
<html lang="en" id="general" class="nojs us" data-root="https://medlineplus.gov/">
|
||
|
||
<head>
|
||
|
||
<meta charset="utf-8" />
|
||
<meta http-equiv="X-UA-Compatible" content="IE=edge,chrome=1" />
|
||
<meta http-equiv="window-target" content="_top" />
|
||
<meta http-equiv="Content-Type" content="text/html; charset=UTF-8" />
|
||
<meta name="viewport" content="width=device-width, initial-scale=1" />
|
||
|
||
|
||
|
||
|
||
|
||
<link rel="canonical" href="https://medlineplus.gov/genetics/condition-h/" />
|
||
|
||
|
||
|
||
|
||
<link href="https://medlineplus.gov/genetics/condition-h/" hreflang="x-default" rel="alternate">
|
||
|
||
|
||
|
||
|
||
<meta name="ac-dictionary" content="medlineplus-ac-dictionary" />
|
||
|
||
|
||
|
||
|
||
|
||
<link rel="shortcut icon" href="https://medlineplus.gov/images/favicon.ico" type="image/x-icon" />
|
||
<link rel="apple-touch-icon" href="https://medlineplus.gov/images/touch-icon.png" />
|
||
|
||
|
||
<meta property="fb:app_id" content="1042245625821448" />
|
||
|
||
|
||
|
||
<meta property="og:title" content="MedlinePlus: Genetic Conditions: H" />
|
||
<meta property="og:url" content="https://medlineplus.gov/genetics/condition-h/" />
|
||
|
||
|
||
|
||
<meta property="og:image" content="https://medlineplus.gov/images/GeneticCondition_Share.jpg" />
|
||
|
||
|
||
|
||
|
||
|
||
|
||
|
||
|
||
|
||
|
||
|
||
<title>MedlinePlus: Genetic Conditions: H</title>
|
||
|
||
<link rel="stylesheet" href="https://medlineplus.gov/css/common_new.css?1738956701052" />
|
||
<!--[if IE 8]> <link rel="stylesheet" href="https://medlineplus.gov/css/ie8/common.css"> <![endif]-->
|
||
<link rel="stylesheet" href="https://medlineplus.gov/uswds/css/uswds_styles.css" />
|
||
|
||
<link rel="stylesheet" href="https://medlineplus.gov/utilities/lostatic.css">
|
||
|
||
|
||
|
||
<script type="text/javascript">document.getElementsByTagName('html')[0].className = document.getElementsByTagName('html')[0].className.replace( /(?:^|\s)nojs(?!\S)/g , '').trim();</script>
|
||
<script src="https://medlineplus.gov/uswds/js/uswds-init.min.js" type="text/javascript"></script>
|
||
|
||
|
||
|
||
|
||
<script>(function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':
|
||
new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],
|
||
j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src=
|
||
'https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);
|
||
})(window,document,'script','dataLayer','GTM-MMVM77');</script>
|
||
</head>
|
||
|
||
<body>
|
||
|
||
<noscript><iframe src="https://www.googletagmanager.com/ns.html?id=GTM-MMVM77"
|
||
height="0" width="0" style="display:none;visibility:hidden" title="googletagmanager"></iframe></noscript>
|
||
|
||
|
||
|
||
<a name="top" id="top"></a>
|
||
<a class="hide-offscreen" href="#start">Skip navigation</a>
|
||
|
||
|
||
|
||
<section
|
||
class="usa-banner"
|
||
aria-label="Official website of the United States government"
|
||
>
|
||
<div class="usa-accordion">
|
||
<header class="usa-banner__header">
|
||
<div class="usa-banner__inner">
|
||
<div class="grid-col-auto">
|
||
<img
|
||
aria-hidden="true"
|
||
class="usa-banner__header-flag"
|
||
src="https://medlineplus.gov/uswds/img/us_flag_small.png"
|
||
alt=""
|
||
/>
|
||
</div>
|
||
<div class="grid-col-fill tablet:grid-col-auto" aria-hidden="true">
|
||
<p class="usa-banner__header-text">
|
||
An official website of the United States government
|
||
</p>
|
||
<p class="usa-banner__header-action">Here’s how you know</p>
|
||
</div>
|
||
<button
|
||
type="button"
|
||
class="usa-accordion__button usa-banner__button"
|
||
aria-expanded="false"
|
||
aria-controls="gov-banner-default-default"
|
||
>
|
||
<span class="usa-banner__button-text">Here’s how you know</span>
|
||
</button>
|
||
</div>
|
||
</header>
|
||
<div
|
||
class="usa-banner__content usa-accordion__content"
|
||
id="gov-banner-default-default"
|
||
>
|
||
<div class="grid-row grid-gap-lg">
|
||
<div class="usa-banner__guidance tablet:grid-col-6">
|
||
<img
|
||
class="usa-banner__icon usa-media-block__img"
|
||
src="https://medlineplus.gov/uswds/img/icon-dot-gov.svg"
|
||
role="img"
|
||
alt=""
|
||
aria-hidden="true"
|
||
/>
|
||
<div class="usa-media-block__body">
|
||
<p>
|
||
<strong>Official websites use .gov</strong><br />A
|
||
<strong>.gov</strong> website belongs to an official government
|
||
organization in the United States.
|
||
</p>
|
||
</div>
|
||
</div>
|
||
<div class="usa-banner__guidance tablet:grid-col-6">
|
||
<img
|
||
class="usa-banner__icon usa-media-block__img"
|
||
src="https://medlineplus.gov/uswds/img/icon-https.svg"
|
||
role="img"
|
||
alt=""
|
||
aria-hidden="true"
|
||
/>
|
||
<div class="usa-media-block__body">
|
||
<p>
|
||
<strong>Secure .gov websites use HTTPS</strong><br />A
|
||
<strong>lock</strong> (
|
||
<span class="icon-lock"
|
||
><svg
|
||
xmlns="http://www.w3.org/2000/svg"
|
||
width="52"
|
||
height="64"
|
||
viewBox="0 0 52 64"
|
||
class="usa-banner__lock-image"
|
||
role="img"
|
||
aria-labelledby="banner-lock-description-default"
|
||
focusable="false"
|
||
>
|
||
<title id="banner-lock-title-default">Lock</title>
|
||
<desc id="banner-lock-description-default">Locked padlock icon</desc>
|
||
<path
|
||
fill="#000000"
|
||
fill-rule="evenodd"
|
||
d="M26 0c10.493 0 19 8.507 19 19v9h3a4 4 0 0 1 4 4v28a4 4 0 0 1-4 4H4a4 4 0 0 1-4-4V32a4 4 0 0 1 4-4h3v-9C7 8.507 15.507 0 26 0zm0 8c-5.979 0-10.843 4.77-10.996 10.712L15 19v9h22v-9c0-6.075-4.925-11-11-11z"
|
||
/>
|
||
</svg> </span
|
||
>) or <strong>https://</strong> means you’ve safely connected to
|
||
the .gov website. Share sensitive information only on official,
|
||
secure websites.
|
||
</p>
|
||
</div>
|
||
</div>
|
||
</div>
|
||
</div>
|
||
</div>
|
||
</section>
|
||
|
||
|
||
<div id="mplus-wrap">
|
||
<header>
|
||
<div id="mplus-header">
|
||
|
||
<div id="mplus-orgs">
|
||
<a href="https://www.nih.gov/" class="nih-org" target="_blank" title="National Institutes of Health">
|
||
<img class="nihlogo" src="https://medlineplus.gov/images/nihlogo.png" alt="National Institutes of Health"/>
|
||
</a><a href="https://www.nlm.nih.gov/" target="_blank"> National Library of Medicine</a>
|
||
</div>
|
||
|
||
|
||
<div id="mplus-logo" class="years-25">
|
||
<a href="https://medlineplus.gov/">
|
||
<img alt="MedlinePlus Trusted Health Information for You" title="MedlinePlus Trusted Health Information for You" src="https://medlineplus.gov/images/m_logo_25.png"/>
|
||
</a>
|
||
</div>
|
||
|
||
|
||
<div id="mplus-nav">
|
||
|
||
<div aria-live="polite" class="sm-live-area hide-offscreen"></div>
|
||
<button id="sm-menu-btn" class="navmenu-btn" title="Menu" role="button" aria-controls="mplus-menu-list" type="submit">Menu<span class="icon icon-nav-menu"></span></button>
|
||
<ul id="mplus-menu-list" class="nav-list">
|
||
<li><a href="https://medlineplus.gov/healthtopics.html">Health Topics</a></li>
|
||
<li><a href="https://medlineplus.gov/druginformation.html">Drugs & Supplements</a></li>
|
||
<li><a href="https://medlineplus.gov/genetics/">Genetics</a></li>
|
||
<li><a href="https://medlineplus.gov/lab-tests/">Medical Tests</a></li>
|
||
<li><a href="https://medlineplus.gov/encyclopedia.html">Medical Encyclopedia</a></li>
|
||
<li><a href="https://medlineplus.gov/about/">About MedlinePlus</a></li>
|
||
</ul><button id="sm-search-btn" class="navmenu-btn" title="Search" role="button" aria-controls="mplus-search" type="submit"><span class="hide-offscreen"></span>Search<span class="icon icon-nav-search"></span></button>
|
||
|
||
<div class="top-1">
|
||
|
||
<form id="mplus-search" method="get" action="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta" title="Search MedlinePlus" target="_self">
|
||
|
||
<input type="hidden" name="v:project" value="medlineplus"/>
|
||
<input type="hidden" name="v:sources" value="medlineplus-bundle"/>
|
||
|
||
<div class="form-box text-combo">
|
||
<div class="form-area"><label class="hide-offscreen" for="searchtext_primary">Search MedlinePlus</label>
|
||
<input id="searchtext_primary" class="form-text" type="text" placeholder="Search MedlinePlus" alt="#Site Search input" title="Site Search input" maxlength="400" size="40" name="query" autocomplete="off" role="textbox" aria-autocomplete="list" aria-haspopup="true"/>
|
||
</div>
|
||
<div class="button-area">
|
||
<button class="form-btn" title="Search MedlinePlus" alt="Search MedlinePlus" type="submit">GO</button>
|
||
</div>
|
||
</div>
|
||
</form>
|
||
|
||
<div class="secondarynav">
|
||
<ul class="nav-list">
|
||
<li><a href="https://medlineplus.gov/about/"><span>About MedlinePlus</span></a></li>
|
||
<li><a href="https://medlineplus.gov/whatsnew/">What's New</a></li>
|
||
<li><a href="https://medlineplus.gov/sitemap.html"><span>Site Map</span></a></li>
|
||
|
||
|
||
<li><a href="https://support.nlm.nih.gov/knowledgebase/category/?id=CAT-01231&category=medlineplus&from=https%3A//medlineplus.gov/genetics/condition-h/" target="_blank"><span>Customer Support</span></a></li>
|
||
|
||
</ul>
|
||
</div>
|
||
|
||
</div>
|
||
<div id="mplus-nav-bar">
|
||
<ul class="nav-list">
|
||
<li><a href="https://medlineplus.gov/healthtopics.html">Health Topics</a></li><li><a href="https://medlineplus.gov/druginformation.html">Drugs & Supplements</a></li><li><a href="https://medlineplus.gov/genetics/">Genetics</a></li><li><a href="https://medlineplus.gov/lab-tests/">Medical Tests</a></li><li><a href="https://medlineplus.gov/encyclopedia.html">Medical Encyclopedia</a></li>
|
||
</ul>
|
||
</div>
|
||
|
||
|
||
</div>
|
||
</div>
|
||
</header>
|
||
|
||
<div id="mplus-content">
|
||
|
||
<div id="breadcrumbs">
|
||
<div itemprop="breadcrumb" itemscope="" itemtype="http://schema.org/BreadcrumbList">
|
||
<span class="hide-offscreen">You Are Here:</span>
|
||
<div itemscope itemprop="itemListElement" itemtype="http://schema.org/ListItem">
|
||
<a href="https://medlineplus.gov/" itemprop="item"><span itemprop="name">Home</span></a>
|
||
→
|
||
<meta itemprop="position" content="1"/>
|
||
</div>
|
||
|
||
|
||
<div itemscope itemprop="itemListElement" itemtype="http://schema.org/ListItem">
|
||
<a href="https://medlineplus.gov/genetics/" itemprop="item"><span itemprop="name">Genetics</span></a>
|
||
→
|
||
<meta itemprop="position" content="2"/>
|
||
</div>
|
||
|
||
|
||
|
||
<div>
|
||
<span>Genetic Conditions: H</span>
|
||
</div>
|
||
|
||
|
||
</div>
|
||
</div>
|
||
<span class="page-url print-only">URL of this page: https://medlineplus.gov/genetics/condition-h/</span>
|
||
|
||
<div >
|
||
|
||
<article>
|
||
<div class="page-info">
|
||
<div class="page-title">
|
||
<a name="start" id="start"></a>
|
||
<h1>Genetic Conditions: H</h1>
|
||
</div>
|
||
<div class="page-actions"></div>
|
||
<noscript><span class="js-disabled-message">To use the sharing features on this page, please enable JavaScript.</span></noscript>
|
||
</div>
|
||
<div class="main-one">
|
||
|
||
<section>
|
||
<p>Explore the signs and symptoms, genetic cause, and inheritance pattern of various health conditions.</p>
|
||
<nav role="navigation">
|
||
<div class="alphanav bluearea section azindex">
|
||
<div class="section-header">
|
||
<div class="section-title">
|
||
<span class='blue-label'>Other genetic conditions A-Z</span>
|
||
</div>
|
||
<div class="section-button">
|
||
<button tabindex="0" aria-pressed="false" title="Expand Section" role="button" aria-controls="az-section" type="submit">
|
||
<span class="icon icon-section-action"></span>
|
||
<span class="hide-offscreen">Expand Section</span>
|
||
</button>
|
||
</div>
|
||
<div class="sm-live-area hide-offscreen" aria-live="polite"></div>
|
||
</div>
|
||
<div id="az-section" class="section-body">
|
||
<ul class="alpha-links">
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-0/" data-alpha="0-9">0-9</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/" data-alpha="A">A</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-b/" data-alpha="B">B</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-c/" data-alpha="C">C</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-d/" data-alpha="D">D</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-e/" data-alpha="E">E</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-f/" data-alpha="F">F</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-g/" data-alpha="G">G</a></li>
|
||
|
||
|
||
|
||
<li><span class="active">H</span></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-i/" data-alpha="I">I</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-j/" data-alpha="J">J</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-k/" data-alpha="K">K</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-l/" data-alpha="L">L</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-m/" data-alpha="M">M</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-n/" data-alpha="N">N</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-o/" data-alpha="O">O</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-p/" data-alpha="P">P</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-q/" data-alpha="Q">Q</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-r/" data-alpha="R">R</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-s/" data-alpha="S">S</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-t/" data-alpha="T">T</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-u/" data-alpha="U">U</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-v/" data-alpha="V">V</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-w/" data-alpha="W">W</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-x/" data-alpha="X">X</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-y/" data-alpha="Y">Y</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-z/" data-alpha="Z">Z</a></li>
|
||
|
||
|
||
</ul>
|
||
</div>
|
||
</div>
|
||
</nav>
|
||
</section>
|
||
|
||
<section>
|
||
|
||
<ul class="withident breaklist">
|
||
|
||
<li>H-CK, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/isolated-hyperckemia/">Isolated hyperCKemia</a></li>
|
||
|
||
|
||
<li>Haberland syndrome (formerly), <i>see</i> <a href="https://medlineplus.gov/genetics/condition/encephalocraniocutaneous-lipomatosis/">Encephalocraniocutaneous lipomatosis</a></li>
|
||
|
||
|
||
<li>HAD deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/3-hydroxyacyl-coa-dehydrogenase-deficiency/">3-hydroxyacyl-CoA dehydrogenase deficiency</a></li>
|
||
|
||
|
||
<li>Haddad syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/congenital-central-hypoventilation-syndrome/">Congenital central hypoventilation syndrome</a></li>
|
||
|
||
|
||
<li>HADH deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/3-hydroxyacyl-coa-dehydrogenase-deficiency/">3-hydroxyacyl-CoA dehydrogenase deficiency</a></li>
|
||
|
||
|
||
<li>HADHSC deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/3-hydroxyacyl-coa-dehydrogenase-deficiency/">3-hydroxyacyl-CoA dehydrogenase deficiency</a></li>
|
||
|
||
|
||
<li>HAE, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-angioedema/">Hereditary angioedema</a></li>
|
||
|
||
|
||
<li>Haemochromatosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hemochromatosis/">Hereditary hemochromatosis</a></li>
|
||
|
||
|
||
<li>Haemophilia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hemophilia/">Hemophilia</a></li>
|
||
|
||
|
||
<li>Haemophilia C, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/factor-xi-deficiency/">Factor XI deficiency</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hailey-hailey-disease/">Hailey-Hailey disease</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hajdu-cheney-syndrome/">Hajdu-Cheney syndrome</a></li>
|
||
|
||
<li>HAL deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/histidinemia/">Histidinemia</a></li>
|
||
|
||
|
||
<li>Hall-Hittner syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/charge-syndrome/">CHARGE syndrome</a></li>
|
||
|
||
|
||
<li>Hall-Pallister syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pallister-hall-syndrome/">Pallister-Hall syndrome</a></li>
|
||
|
||
|
||
<li>Hallgren syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/usher-syndrome/">Usher syndrome</a></li>
|
||
|
||
|
||
<li>Hallux abductovalgus, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/bunion/">Bunion</a></li>
|
||
|
||
|
||
<li>Hallux duplication, postaxial polydactyly, and absence of corpus callosum, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/acrocallosal-syndrome/">Acrocallosal syndrome</a></li>
|
||
|
||
|
||
<li>Hallux valgus, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/bunion/">Bunion</a></li>
|
||
|
||
|
||
<li>Hamel cerebropalatocardiac syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/renpenning-syndrome/">Renpenning syndrome</a></li>
|
||
|
||
|
||
<li>HANAC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-angiopathy-with-nephropathy-aneurysms-and-muscle-cramps-syndrome/">Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome</a></li>
|
||
|
||
|
||
<li>HANAC syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-angiopathy-with-nephropathy-aneurysms-and-muscle-cramps-syndrome/">Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hand-foot-genital-syndrome/">Hand-foot-genital syndrome</a></li>
|
||
|
||
<li>Hand-foot-uterus syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hand-foot-genital-syndrome/">Hand-foot-genital syndrome</a></li>
|
||
|
||
|
||
<li>HANE, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-angioedema/">Hereditary angioedema</a></li>
|
||
|
||
|
||
<li>Hansen disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/leprosy/">Leprosy</a></li>
|
||
|
||
|
||
<li>Hansen's disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/leprosy/">Leprosy</a></li>
|
||
|
||
|
||
<li>Happle syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/x-linked-chondrodysplasia-punctata-2/">X-linked chondrodysplasia punctata 2</a></li>
|
||
|
||
|
||
<li>HARD syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/walker-warburg-syndrome/">Walker-Warburg syndrome</a></li>
|
||
|
||
|
||
<li>Harlequin baby syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/harlequin-ichthyosis/">Harlequin ichthyosis</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/harlequin-ichthyosis/">Harlequin ichthyosis</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hartnup-disease/">Hartnup disease</a></li>
|
||
|
||
<li>Hartnup disorder, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hartnup-disease/">Hartnup disease</a></li>
|
||
|
||
|
||
<li>Hartnup's disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hartnup-disease/">Hartnup disease</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hartsfield-syndrome/">Hartsfield syndrome</a></li>
|
||
|
||
<li>Hartsfield-Bixler-Demyer syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hartsfield-syndrome/">Hartsfield syndrome</a></li>
|
||
|
||
|
||
<li>Hashimoto disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hashimotos-disease/">Hashimoto's disease</a></li>
|
||
|
||
|
||
<li>Hashimoto struma, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hashimotos-disease/">Hashimoto's disease</a></li>
|
||
|
||
|
||
<li>Hashimoto syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hashimotos-disease/">Hashimoto's disease</a></li>
|
||
|
||
|
||
<li>Hashimoto thyroidosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hashimotos-disease/">Hashimoto's disease</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hashimotos-disease/">Hashimoto's disease</a></li>
|
||
|
||
<li>Hashimoto-Pritzger disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/langerhans-cell-histiocytosis/">Langerhans cell histiocytosis</a></li>
|
||
|
||
|
||
<li>hATTR, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/transthyretin-amyloidosis/">Transthyretin amyloidosis</a></li>
|
||
|
||
|
||
<li>HAV, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/bunion/">Bunion</a></li>
|
||
|
||
|
||
<li>Haw River syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dentatorubral-pallidoluysian-atrophy/">Dentatorubral-pallidoluysian atrophy</a></li>
|
||
|
||
|
||
<li>Hay-Wells syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ankyloblepharon-ectodermal-defects-cleft-lip-palate-syndrome/">Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome</a></li>
|
||
|
||
|
||
<li>HBBD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/progressive-familial-heart-block/">Progressive familial heart block</a></li>
|
||
|
||
|
||
<li>HbS disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/sickle-cell-disease/">Sickle cell disease</a></li>
|
||
|
||
|
||
<li>HBSL, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypomyelination-with-brainstem-and-spinal-cord-involvement-and-leg-spasticity/">Hypomyelination with brainstem and spinal cord involvement and leg spasticity</a></li>
|
||
|
||
|
||
<li>HC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hemochromatosis/">Hereditary hemochromatosis</a></li>
|
||
|
||
|
||
<li>HCAHC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pol-iii-related-leukodystrophy/">Pol III-related leukodystrophy</a></li>
|
||
|
||
|
||
<li>HCC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypomyelination-and-congenital-cataract/">Hypomyelination and congenital cataract</a></li>
|
||
|
||
|
||
<li>HCH, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypochondroplasia/">Hypochondroplasia</a></li>
|
||
|
||
|
||
<li>HCHWA-D, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-cerebral-amyloid-angiopathy/">Hereditary cerebral amyloid angiopathy</a></li>
|
||
|
||
|
||
<li>HCHWA-I, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-cerebral-amyloid-angiopathy/">Hereditary cerebral amyloid angiopathy</a></li>
|
||
|
||
|
||
<li>HCM, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hypertrophic-cardiomyopathy/">Familial hypertrophic cardiomyopathy</a></li>
|
||
|
||
|
||
<li>HDDD1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/grn-related-frontotemporal-lobar-degeneration/">GRN-related frontotemporal lobar degeneration</a></li>
|
||
|
||
|
||
<li>HDDD2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/grn-related-frontotemporal-lobar-degeneration/">GRN-related frontotemporal lobar degeneration</a></li>
|
||
|
||
|
||
<li>HDGC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-diffuse-gastric-cancer/">Hereditary diffuse gastric cancer</a></li>
|
||
|
||
|
||
<li>HDL, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/huntingtons-disease-like/">Huntington's disease-like</a></li>
|
||
|
||
|
||
<li>HDL deficiency, type 2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hdl-deficiency/">Familial HDL deficiency</a></li>
|
||
|
||
|
||
<li>HDL lipoprotein deficiency disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tangier-disease/">Tangier disease</a></li>
|
||
|
||
|
||
<li>HDL syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/huntingtons-disease-like/">Huntington's disease-like</a></li>
|
||
|
||
|
||
<li>HDLD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hdl-deficiency/">Familial HDL deficiency</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/head-and-neck-squamous-cell-carcinoma/">Head and neck squamous cell carcinoma</a></li>
|
||
|
||
<li>Headache migraine, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/migraine/">Migraine</a></li>
|
||
|
||
|
||
<li>Headache migrainous, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/migraine/">Migraine</a></li>
|
||
|
||
|
||
<li>Hearing loss, age-related, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/age-related-hearing-loss/">Age-related hearing loss</a></li>
|
||
|
||
|
||
<li>Heart-hand syndrome, type 1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/holt-oram-syndrome/">Holt-Oram syndrome</a></li>
|
||
|
||
|
||
<li>HED, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypohidrotic-ectodermal-dysplasia/">Hypohidrotic ectodermal dysplasia</a></li>
|
||
|
||
|
||
<li>HED-ID, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/anhidrotic-ectodermal-dysplasia-with-immune-deficiency/">Anhidrotic ectodermal dysplasia with immune deficiency</a></li>
|
||
|
||
|
||
<li>HED2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/clouston-syndrome/">Clouston syndrome</a></li>
|
||
|
||
|
||
<li>Helsmoortel-van der Aa syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/adnp-syndrome/">ADNP syndrome</a></li>
|
||
|
||
|
||
<li>HEM dysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/greenberg-dysplasia/">Greenberg dysplasia</a></li>
|
||
|
||
|
||
<li>HEM skeletal dysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/greenberg-dysplasia/">Greenberg dysplasia</a></li>
|
||
|
||
|
||
<li>Hemangiomata with dyschondroplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/maffucci-syndrome/">Maffucci syndrome</a></li>
|
||
|
||
|
||
<li>Hemangiomatosis chondrodystrophica, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/maffucci-syndrome/">Maffucci syndrome</a></li>
|
||
|
||
|
||
<li>Hemangiomatous branchial clefts-lip pseudocleft syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/branchio-oculo-facial-syndrome/">Branchio-oculo-facial syndrome</a></li>
|
||
|
||
|
||
<li>Hematoporphyria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/porphyria/">Porphyria</a></li>
|
||
|
||
|
||
<li>Hematuria-nephropathy-deafness syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alport-syndrome/">Alport syndrome</a></li>
|
||
|
||
|
||
<li>Hematuric hereditary nephritis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alport-syndrome/">Alport syndrome</a></li>
|
||
|
||
|
||
<li>Hemifacial microsomia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/craniofacial-microsomia/">Craniofacial microsomia</a></li>
|
||
|
||
|
||
<li>Hemiplegic migraine, familial, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hemiplegic-migraine/">Familial hemiplegic migraine</a></li>
|
||
|
||
|
||
<li>Hemiplegic-ophthalmoplegic migraine, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hemiplegic-migraine/">Familial hemiplegic migraine</a></li>
|
||
|
||
|
||
<li>Hemochromatosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hemochromatosis/">Hereditary hemochromatosis</a></li>
|
||
|
||
|
||
<li>Hemoglobin M disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/methemoglobinemia-beta-globin-type/">Methemoglobinemia, beta-globin type</a></li>
|
||
|
||
|
||
<li>Hemoglobin S disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/sickle-cell-disease/">Sickle cell disease</a></li>
|
||
|
||
|
||
<li>Hemoglobinuria, paroxysmal, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/paroxysmal-nocturnal-hemoglobinuria/">Paroxysmal nocturnal hemoglobinuria</a></li>
|
||
|
||
|
||
<li>Hemophagocytic syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hemophagocytic-lymphohistiocytosis/">Familial hemophagocytic lymphohistiocytosis</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hemophilia/">Hemophilia</a></li>
|
||
|
||
<li>Hemophilia C, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/factor-xi-deficiency/">Factor XI deficiency</a></li>
|
||
|
||
|
||
<li>Hemophilia, familial, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hemophilia/">Hemophilia</a></li>
|
||
|
||
|
||
<li>Hemophilia, hereditary, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hemophilia/">Hemophilia</a></li>
|
||
|
||
|
||
<li>Hemorrhagic familial nephritis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alport-syndrome/">Alport syndrome</a></li>
|
||
|
||
|
||
<li>Hemorrhagic hereditary nephritis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alport-syndrome/">Alport syndrome</a></li>
|
||
|
||
|
||
<li>Hemorrhagioparous thrombocytic dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/bernard-soulier-syndrome/">Bernard-Soulier syndrome</a></li>
|
||
|
||
|
||
<li>Hennekam lymphangiectasia-lymphedema syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hennekam-syndrome/">Hennekam syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hennekam-syndrome/">Hennekam syndrome</a></li>
|
||
|
||
<li>Hepatic AGT deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/primary-hyperoxaluria/">Primary hyperoxaluria</a></li>
|
||
|
||
|
||
<li>Hepatic ductular hypoplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alagille-syndrome/">Alagille syndrome</a></li>
|
||
|
||
|
||
<li>Hepatic glycogen phosphorylase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glycogen-storage-disease-type-vi/">Glycogen storage disease type VI</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hepatic-lipase-deficiency/">Hepatic lipase deficiency</a></li>
|
||
|
||
<li>Hepatic methionine adenosyltransferase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypermethioninemia/">Hypermethioninemia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hepatic-veno-occlusive-disease-with-immunodeficiency/">Hepatic veno-occlusive disease with immunodeficiency</a></li>
|
||
|
||
<li>Hepatic venoocclusive disease with immunodeficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hepatic-veno-occlusive-disease-with-immunodeficiency/">Hepatic veno-occlusive disease with immunodeficiency</a></li>
|
||
|
||
|
||
<li>Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/combined-oxidative-phosphorylation-deficiency-1/">Combined oxidative phosphorylation deficiency 1</a></li>
|
||
|
||
|
||
<li>Hepatofacioneurocardiovertebral syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alagille-syndrome/">Alagille syndrome</a></li>
|
||
|
||
|
||
<li>Hepatolenticular degeneration syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/wilson-disease/">Wilson disease</a></li>
|
||
|
||
|
||
<li>Hepatorenal form of glycogen storage disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glycogen-storage-disease-type-i/">Glycogen storage disease type I</a></li>
|
||
|
||
|
||
<li>Hepatorenal glycogenosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glycogen-storage-disease-type-i/">Glycogen storage disease type I</a></li>
|
||
|
||
|
||
<li>Hereditary aldosteronism, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hyperaldosteronism/">Familial hyperaldosteronism</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-angioedema/">Hereditary angioedema</a></li>
|
||
|
||
<li>Hereditary angioneurotic edema, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-angioedema/">Hereditary angioedema</a></li>
|
||
|
||
|
||
<li>Hereditary angiopathy with nephropathy, aneurysm, and muscle cramps syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-angiopathy-with-nephropathy-aneurysms-and-muscle-cramps-syndrome/">Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-angiopathy-with-nephropathy-aneurysms-and-muscle-cramps-syndrome/">Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-antithrombin-deficiency/">Hereditary antithrombin deficiency</a></li>
|
||
|
||
<li>Hereditary arthro-ophthalmo-dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/stickler-syndrome/">Stickler syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary arthro-ophthalmopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/stickler-syndrome/">Stickler syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary brachial plexus neuropathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-neuralgic-amyotrophy/">Hereditary neuralgic amyotrophy</a></li>
|
||
|
||
|
||
<li>Hereditary bundle branch defect, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/progressive-familial-heart-block/">Progressive familial heart block</a></li>
|
||
|
||
|
||
<li>Hereditary bundle branch system defect, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/progressive-familial-heart-block/">Progressive familial heart block</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-cerebral-amyloid-angiopathy/">Hereditary cerebral amyloid angiopathy</a></li>
|
||
|
||
<li>Hereditary cerebral hemorrhage with amyloidosis-Dutch type, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-cerebral-amyloid-angiopathy/">Hereditary cerebral amyloid angiopathy</a></li>
|
||
|
||
|
||
<li>Hereditary cerebral hemorrhage with amyloidosis-Icelandic type, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-cerebral-amyloid-angiopathy/">Hereditary cerebral amyloid angiopathy</a></li>
|
||
|
||
|
||
<li>Hereditary ceruloplasmin deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/aceruloplasminemia/">Aceruloplasminemia</a></li>
|
||
|
||
|
||
<li>Hereditary chronic pancreatitis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-pancreatitis/">Hereditary pancreatitis</a></li>
|
||
|
||
|
||
<li>Hereditary cranium bifidum, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/enlarged-parietal-foramina/">Enlarged parietal foramina</a></li>
|
||
|
||
|
||
<li>Hereditary dementia, multi-infarct type, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cerebral-autosomal-dominant-arteriopathy-with-subcortical-infarcts-and-leukoencephalopathy/">Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy</a></li>
|
||
|
||
|
||
<li>Hereditary desmoid disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/desmoid-tumor/">Desmoid tumor</a></li>
|
||
|
||
|
||
<li>Hereditary diffuse gastric adenocarcinoma, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-diffuse-gastric-cancer/">Hereditary diffuse gastric cancer</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-diffuse-gastric-cancer/">Hereditary diffuse gastric cancer</a></li>
|
||
|
||
<li>Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/adult-onset-leukoencephalopathy-with-axonal-spheroids-and-pigmented-glia/">Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia</a></li>
|
||
|
||
|
||
<li>Hereditary dysphasic disinhibition dementia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/grn-related-frontotemporal-lobar-degeneration/">GRN-related frontotemporal lobar degeneration</a></li>
|
||
|
||
|
||
<li>Hereditary dystopic lipidosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fabry-disease/">Fabry disease</a></li>
|
||
|
||
|
||
<li>Hereditary epithelial dysplasia of retina, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/leber-congenital-amaurosis/">Leber congenital amaurosis</a></li>
|
||
|
||
|
||
<li>Hereditary erythrocytosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-erythrocytosis/">Familial erythrocytosis</a></li>
|
||
|
||
|
||
<li>Hereditary essential tremor, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/essential-tremor/">Essential tremor</a></li>
|
||
|
||
|
||
<li>Hereditary factor I deficiency disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/complement-factor-i-deficiency/">Complement factor I deficiency</a></li>
|
||
|
||
|
||
<li>Hereditary familial congenital hemorrhagic nephritis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alport-syndrome/">Alport syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary ferritinopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/neuroferritinopathy/">Neuroferritinopathy</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-fibrosing-poikiloderma-with-tendon-contractures-myopathy-and-pulmonary-fibrosis/">Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-folate-malabsorption/">Hereditary folate malabsorption</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-fructose-intolerance/">Hereditary fructose intolerance</a></li>
|
||
|
||
<li>Hereditary glaucoma, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/early-onset-glaucoma/">Early-onset glaucoma</a></li>
|
||
|
||
|
||
<li>Hereditary gynecomastia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/aromatase-excess-syndrome/">Aromatase excess syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary haemochromatosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hemochromatosis/">Hereditary hemochromatosis</a></li>
|
||
|
||
|
||
<li>Hereditary hematuria syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alport-syndrome/">Alport syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-hemochromatosis/">Hereditary hemochromatosis</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-hemorrhagic-telangiectasia/">Hereditary hemorrhagic telangiectasia</a></li>
|
||
|
||
<li>Hereditary hemorrhagic thrombasthenia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glanzmann-thrombasthenia/">Glanzmann thrombasthenia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-hyperekplexia/">Hereditary hyperekplexia</a></li>
|
||
|
||
<li>Hereditary hyperferritinemia with congenital cataracts, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperferritinemia-cataract-syndrome/">Hyperferritinemia-cataract syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary hyperferritinemia-cataract syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperferritinemia-cataract-syndrome/">Hyperferritinemia-cataract syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary hyperparathyroidism-jaw tumor syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperparathyroidism-jaw-tumor-syndrome/">Hyperparathyroidism-jaw tumor syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-hypophosphatemic-rickets/">Hereditary hypophosphatemic rickets</a></li>
|
||
|
||
<li>Hereditary inclusion body myopathy type 2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/gne-myopathy/">GNE myopathy</a></li>
|
||
|
||
|
||
<li>Hereditary insensitivity to pain with anhidrosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/congenital-insensitivity-to-pain-with-anhidrosis/">Congenital insensitivity to pain with anhidrosis</a></li>
|
||
|
||
|
||
<li>Hereditary interstitial pyelonephritis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alport-syndrome/">Alport syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary iron-loading anemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/x-linked-sideroblastic-anemia/">X-linked sideroblastic anemia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-leiomyomatosis-and-renal-cell-cancer/">Hereditary leiomyomatosis and renal cell cancer</a></li>
|
||
|
||
<li>Hereditary leiomyomatosis and renal cell carcinoma, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-leiomyomatosis-and-renal-cell-cancer/">Hereditary leiomyomatosis and renal cell cancer</a></li>
|
||
|
||
|
||
<li>Hereditary leukokeratosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/white-sponge-nevus/">White sponge nevus</a></li>
|
||
|
||
|
||
<li>Hereditary lymphedema II, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/meige-disease/">Meige disease</a></li>
|
||
|
||
|
||
<li>Hereditary lymphedema type I, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/milroy-disease/">Milroy disease</a></li>
|
||
|
||
|
||
<li>Hereditary motor and sensory neuropathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-neuropathy-with-liability-to-pressure-palsies/">Hereditary neuropathy with liability to pressure palsies</a></li>
|
||
|
||
|
||
<li>Hereditary motor and sensory neuropathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/charcot-marie-tooth-disease/">Charcot-Marie-Tooth disease</a></li>
|
||
|
||
|
||
<li>Hereditary motor and sensory neuropathy type IV, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/refsum-disease/">Refsum disease</a></li>
|
||
|
||
|
||
<li>Hereditary motor and sensory neuropathy with agenesis of the corpus callosum, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/andermann-syndrome/">Andermann syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary mucosal leukokeratosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/white-sponge-nevus/">White sponge nevus</a></li>
|
||
|
||
|
||
<li>Hereditary multicentric osteolysis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/multicentric-osteolysis-nodulosis-and-arthropathy/">Multicentric osteolysis, nodulosis, and arthropathy</a></li>
|
||
|
||
|
||
<li>Hereditary multiple benign cystic epithelioma, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/multiple-familial-trichoepithelioma/">Multiple familial trichoepithelioma</a></li>
|
||
|
||
|
||
<li>Hereditary multiple exostoses, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-multiple-osteochondromas/">Hereditary multiple osteochondromas</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-multiple-osteochondromas/">Hereditary multiple osteochondromas</a></li>
|
||
|
||
<li>Hereditary myoclonus with progressive distal muscular atrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/spinal-muscular-atrophy-with-progressive-myoclonic-epilepsy/">Spinal muscular atrophy with progressive myoclonic epilepsy</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-myopathy-with-early-respiratory-failure/">Hereditary myopathy with early respiratory failure</a></li>
|
||
|
||
<li>Hereditary myopathy with lactic acidosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/myopathy-with-deficiency-of-iron-sulfur-cluster-assembly-enzyme/">Myopathy with deficiency of iron-sulfur cluster assembly enzyme</a></li>
|
||
|
||
|
||
<li>Hereditary nephritis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alport-syndrome/">Alport syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-neuralgic-amyotrophy/">Hereditary neuralgic amyotrophy</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-neuropathy-with-liability-to-pressure-palsies/">Hereditary neuropathy with liability to pressure palsies</a></li>
|
||
|
||
<li>Hereditary nonpolyposis colorectal cancer, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lynch-syndrome/">Lynch syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary nonpolyposis colorectal neoplasms, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lynch-syndrome/">Lynch syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/triosephosphate-isomerase-deficiency/">Triosephosphate isomerase deficiency</a></li>
|
||
|
||
|
||
<li>Hereditary oligophrenic cerebello-lental degeneration, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/marinesco-sjogren-syndrome/">Marinesco-Sjögren syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary onycho-osteodysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/nail-patella-syndrome/">Nail-patella syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary opalescent dentin, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dentinogenesis-imperfecta/">Dentinogenesis imperfecta</a></li>
|
||
|
||
|
||
<li>Hereditary optic neuroretinopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/leber-hereditary-optic-neuropathy/">Leber hereditary optic neuropathy</a></li>
|
||
|
||
|
||
<li>Hereditary oral keratosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/white-sponge-nevus/">White sponge nevus</a></li>
|
||
|
||
|
||
<li>Hereditary osteo-onychodysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/nail-patella-syndrome/">Nail-patella syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary osteodysplasia with acro-osteolysis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hajdu-cheney-syndrome/">Hajdu-Cheney syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-pancreatitis/">Hereditary pancreatitis</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-paraganglioma-pheochromocytoma/">Hereditary paraganglioma-pheochromocytoma</a></li>
|
||
|
||
<li>Hereditary paraganglioma-pheochromocytoma syndromes, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-paraganglioma-pheochromocytoma/">Hereditary paraganglioma-pheochromocytoma</a></li>
|
||
|
||
|
||
<li>Hereditary pheochromocytoma-paraganglioma, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-paraganglioma-pheochromocytoma/">Hereditary paraganglioma-pheochromocytoma</a></li>
|
||
|
||
|
||
<li>Hereditary pressure sensitive neuropathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-neuropathy-with-liability-to-pressure-palsies/">Hereditary neuropathy with liability to pressure palsies</a></li>
|
||
|
||
|
||
<li>Hereditary progressive dystonia with marked diurnal fluctuation, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dopa-responsive-dystonia/">Dopa-responsive dystonia</a></li>
|
||
|
||
|
||
<li>Hereditary pulmonary emphysema, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alpha-1-antitrypsin-deficiency/">Alpha-1 antitrypsin deficiency</a></li>
|
||
|
||
|
||
<li>Hereditary renal hypouricemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/renal-hypouricemia/">Renal hypouricemia</a></li>
|
||
|
||
|
||
<li>Hereditary resistance to activated protein C, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/factor-v-leiden-thrombophilia/">Factor V Leiden thrombophilia</a></li>
|
||
|
||
|
||
<li>Hereditary retinal aplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/leber-congenital-amaurosis/">Leber congenital amaurosis</a></li>
|
||
|
||
|
||
<li>Hereditary sclerosing poikiloderma with tendon and pulmonary involvement, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-fibrosing-poikiloderma-with-tendon-contractures-myopathy-and-pulmonary-fibrosis/">Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis</a></li>
|
||
|
||
|
||
<li>Hereditary sensory and autonomic neuropathy type 1 with dementia and hearing loss, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ie/">Hereditary sensory and autonomic neuropathy type IE</a></li>
|
||
|
||
|
||
<li>Hereditary sensory and autonomic neuropathy type 2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ii/">Hereditary sensory and autonomic neuropathy type II</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ie/">Hereditary sensory and autonomic neuropathy type IE</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ii/">Hereditary sensory and autonomic neuropathy type II</a></li>
|
||
|
||
<li>Hereditary sensory and autonomic neuropathy type IV, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/congenital-insensitivity-to-pain-with-anhidrosis/">Congenital insensitivity to pain with anhidrosis</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-v/">Hereditary sensory and autonomic neuropathy type V</a></li>
|
||
|
||
<li>Hereditary sensory and autonomic neuropathy, type 4, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/congenital-insensitivity-to-pain-with-anhidrosis/">Congenital insensitivity to pain with anhidrosis</a></li>
|
||
|
||
|
||
<li>Hereditary sensory and autonomic neuropathy, type 5, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-v/">Hereditary sensory and autonomic neuropathy type V</a></li>
|
||
|
||
|
||
<li>Hereditary sensory and autonomic neuropathy, type IA, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-neuropathy-type-ia/">Hereditary sensory neuropathy type IA</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-neuropathy-type-ia/">Hereditary sensory neuropathy type IA</a></li>
|
||
|
||
<li>Hereditary sensory neuropathy type IE, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ie/">Hereditary sensory and autonomic neuropathy type IE</a></li>
|
||
|
||
|
||
<li>Hereditary spastic paraplegia 8, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-8/">Spastic paraplegia type 8</a></li>
|
||
|
||
|
||
<li>Hereditary spastic paraplegia, paraplegin type, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-7/">Spastic paraplegia type 7</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-spherocytosis/">Hereditary spherocytosis</a></li>
|
||
|
||
<li>Hereditary SWI/SNF deficiency syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/rhabdoid-tumor-predisposition-syndrome/">Rhabdoid tumor predisposition syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary syndrome of lumpy scalp, odd ears, and rudimentary nipples, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/scalp-ear-nipple-syndrome/">Scalp-ear-nipple syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary thrombasthenia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glanzmann-thrombasthenia/">Glanzmann thrombasthenia</a></li>
|
||
|
||
|
||
<li>Hereditary thrombophilia due to protein C deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/protein-c-deficiency/">Protein C deficiency</a></li>
|
||
|
||
|
||
<li>Hereditary thrombophilia due to protein S deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/protein-s-deficiency/">Protein S deficiency</a></li>
|
||
|
||
|
||
<li>Hereditary thymine-uraciluria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dihydropyrimidine-dehydrogenase-deficiency/">Dihydropyrimidine dehydrogenase deficiency</a></li>
|
||
|
||
|
||
<li>Hereditary tyrosinemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tyrosinemia/">Tyrosinemia</a></li>
|
||
|
||
|
||
<li>Hereditary unconjugated hyperbilirubinemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/crigler-najjar-syndrome/">Crigler-Najjar syndrome</a></li>
|
||
|
||
|
||
<li>Hereditary unresponsiveness to adrenocorticotropic hormone, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-glucocorticoid-deficiency/">Familial glucocorticoid deficiency</a></li>
|
||
|
||
|
||
<li>Hereditary ventricular hypertrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hypertrophic-cardiomyopathy/">Familial hypertrophic cardiomyopathy</a></li>
|
||
|
||
|
||
<li>Hereditary X-linked recessive spastic paraplegia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-2/">Spastic paraplegia type 2</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hereditary-xanthinuria/">Hereditary xanthinuria</a></li>
|
||
|
||
<li>Heredofamilial neuritis with brachial plexus predilection, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-neuralgic-amyotrophy/">Hereditary neuralgic amyotrophy</a></li>
|
||
|
||
|
||
<li>Heredopathia atactica polyneuritiformis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/refsum-disease/">Refsum disease</a></li>
|
||
|
||
|
||
<li>Heredoretinopathia congenitalis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/leber-congenital-amaurosis/">Leber congenital amaurosis</a></li>
|
||
|
||
|
||
<li>Heritable hypertrophic cardiomyopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hypertrophic-cardiomyopathy/">Familial hypertrophic cardiomyopathy</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hermansky-pudlak-syndrome/">Hermansky-Pudlak syndrome</a></li>
|
||
|
||
<li>Hernia, abdominal, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/abdominal-wall-defect/">Abdominal wall defect</a></li>
|
||
|
||
|
||
<li>Herpes zoster, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/shingles/">Shingles</a></li>
|
||
|
||
|
||
<li>Hers disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glycogen-storage-disease-type-vi/">Glycogen storage disease type VI</a></li>
|
||
|
||
|
||
<li>Heterotaxy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/heterotaxy-syndrome/">Heterotaxy syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/heterotaxy-syndrome/">Heterotaxy syndrome</a></li>
|
||
|
||
<li>Heterotopia, subcortical band, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/subcortical-band-heterotopia/">Subcortical band heterotopia</a></li>
|
||
|
||
|
||
<li>Heterotopic ossification, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/progressive-osseous-heteroplasia/">Progressive osseous heteroplasia</a></li>
|
||
|
||
|
||
<li>Heterozygous OSMED, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/weissenbacher-zweymuller-syndrome/">Weissenbacher-Zweymüller syndrome</a></li>
|
||
|
||
|
||
<li>Heterozygous otospondylomegaepiphyseal dysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/weissenbacher-zweymuller-syndrome/">Weissenbacher-Zweymüller syndrome</a></li>
|
||
|
||
|
||
<li>HexA deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tay-sachs-disease/">Tay-Sachs disease</a></li>
|
||
|
||
|
||
<li>Hexosaminidase A and B deficiency disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/sandhoff-disease/">Sandhoff disease</a></li>
|
||
|
||
|
||
<li>Hexosaminidase A deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tay-sachs-disease/">Tay-Sachs disease</a></li>
|
||
|
||
|
||
<li>Hexosaminidase activator deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/gm2-activator-deficiency/">GM2 activator deficiency</a></li>
|
||
|
||
|
||
<li>Hexosaminidase alpha-subunit deficiency (variant B), <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tay-sachs-disease/">Tay-Sachs disease</a></li>
|
||
|
||
|
||
<li>HFG syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hand-foot-genital-syndrome/">Hand-foot-genital syndrome</a></li>
|
||
|
||
|
||
<li>HFGS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hand-foot-genital-syndrome/">Hand-foot-genital syndrome</a></li>
|
||
|
||
|
||
<li>HFM, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/craniofacial-microsomia/">Craniofacial microsomia</a></li>
|
||
|
||
|
||
<li>HFP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-fibrosing-poikiloderma-with-tendon-contractures-myopathy-and-pulmonary-fibrosis/">Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis</a></li>
|
||
|
||
|
||
<li>HFTC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperphosphatemic-familial-tumoral-calcinosis/">Hyperphosphatemic familial tumoral calcinosis</a></li>
|
||
|
||
|
||
<li>HFU syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hand-foot-genital-syndrome/">Hand-foot-genital syndrome</a></li>
|
||
|
||
|
||
<li>HGPPS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/horizontal-gaze-palsy-with-progressive-scoliosis/">Horizontal gaze palsy with progressive scoliosis</a></li>
|
||
|
||
|
||
<li>HGPRT deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lesch-nyhan-syndrome/">Lesch-Nyhan syndrome</a></li>
|
||
|
||
|
||
<li>HGPS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hutchinson-gilford-progeria-syndrome/">Hutchinson-Gilford progeria syndrome</a></li>
|
||
|
||
|
||
<li>HH, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hemochromatosis/">Hereditary hemochromatosis</a></li>
|
||
|
||
|
||
<li>HHCS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperferritinemia-cataract-syndrome/">Hyperferritinemia-cataract syndrome</a></li>
|
||
|
||
|
||
<li>HHES, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hartsfield-syndrome/">Hartsfield syndrome</a></li>
|
||
|
||
|
||
<li>HHH syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ornithine-translocase-deficiency/">Ornithine translocase deficiency</a></li>
|
||
|
||
|
||
<li>HHT, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hemorrhagic-telangiectasia/">Hereditary hemorrhagic telangiectasia</a></li>
|
||
|
||
|
||
<li>HI, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/harlequin-ichthyosis/">Harlequin ichthyosis</a></li>
|
||
|
||
|
||
<li>HIBM2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/gne-myopathy/">GNE myopathy</a></li>
|
||
|
||
|
||
<li>HID syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hystrix-like-ichthyosis-with-deafness/">Hystrix-like ichthyosis with deafness</a></li>
|
||
|
||
|
||
<li>Hidradenitides, suppurative, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hidradenitis-suppurativa/">Hidradenitis suppurativa</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hidradenitis-suppurativa/">Hidradenitis suppurativa</a></li>
|
||
|
||
<li>Hidradenitis, suppurative, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hidradenitis-suppurativa/">Hidradenitis suppurativa</a></li>
|
||
|
||
|
||
<li>Hidrotic ectodermal dysplasia 2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/clouston-syndrome/">Clouston syndrome</a></li>
|
||
|
||
|
||
<li>High blood pressure, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypertension/">Hypertension</a></li>
|
||
|
||
|
||
<li>High myopia and sensorineural deafness, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/deafness-and-myopia-syndrome/">Deafness and myopia syndrome</a></li>
|
||
|
||
|
||
<li>High myopia-sensorineural deafness syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/deafness-and-myopia-syndrome/">Deafness and myopia syndrome</a></li>
|
||
|
||
|
||
<li>HIGM1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/x-linked-hyper-igm-syndrome/">X-linked hyper IgM syndrome</a></li>
|
||
|
||
|
||
<li>Hippel-Lindau disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/von-hippel-lindau-syndrome/">Von Hippel-Lindau syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hirschsprung-disease/">Hirschsprung disease</a></li>
|
||
|
||
<li>Hirschsprung disease-mental retardation syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mowat-wilson-syndrome/">Mowat-Wilson syndrome</a></li>
|
||
|
||
|
||
<li>Hirschsprung's disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hirschsprung-disease/">Hirschsprung disease</a></li>
|
||
|
||
|
||
<li>HIS deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/histidinemia/">Histidinemia</a></li>
|
||
|
||
|
||
<li>Histidase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/histidinemia/">Histidinemia</a></li>
|
||
|
||
|
||
<li>Histidine ammonia-lyase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/histidinemia/">Histidinemia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/histidinemia/">Histidinemia</a></li>
|
||
|
||
<li>Histidinuria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/histidinemia/">Histidinemia</a></li>
|
||
|
||
|
||
<li>Histiocytic medullary reticulosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/omenn-syndrome/">Omenn syndrome</a></li>
|
||
|
||
|
||
<li>Histiocytosis X, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/langerhans-cell-histiocytosis/">Langerhans cell histiocytosis</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/histiocytosis-lymphadenopathy-plus-syndrome/">Histiocytosis-lymphadenopathy plus syndrome</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hivep2-related-intellectual-disability/">HIVEP2-related intellectual disability</a></li>
|
||
|
||
<li>HJCYS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hajdu-cheney-syndrome/">Hajdu-Cheney syndrome</a></li>
|
||
|
||
|
||
<li>HL deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hepatic-lipase-deficiency/">Hepatic lipase deficiency</a></li>
|
||
|
||
|
||
<li>HLA class I deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/bare-lymphocyte-syndrome-type-i/">Bare lymphocyte syndrome type I</a></li>
|
||
|
||
|
||
<li>HLAH, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hemochromatosis/">Hereditary hemochromatosis</a></li>
|
||
|
||
|
||
<li>HLCS deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/holocarboxylase-synthetase-deficiency/">Holocarboxylase synthetase deficiency</a></li>
|
||
|
||
|
||
<li>HLD1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pelizaeus-merzbacher-disease/">Pelizaeus-Merzbacher disease</a></li>
|
||
|
||
|
||
<li>HLD2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pelizaeus-merzbacher-like-disease-type-1/">Pelizaeus-Merzbacher-like disease type 1</a></li>
|
||
|
||
|
||
<li>HLD7, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pol-iii-related-leukodystrophy/">Pol III-related leukodystrophy</a></li>
|
||
|
||
|
||
<li>HLD8, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pol-iii-related-leukodystrophy/">Pol III-related leukodystrophy</a></li>
|
||
|
||
|
||
<li>HLRCC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-leiomyomatosis-and-renal-cell-cancer/">Hereditary leiomyomatosis and renal cell cancer</a></li>
|
||
|
||
|
||
<li>HMCS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mckusick-kaufman-syndrome/">McKusick-Kaufman syndrome</a></li>
|
||
|
||
|
||
<li>HMERF, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-myopathy-with-early-respiratory-failure/">Hereditary myopathy with early respiratory failure</a></li>
|
||
|
||
|
||
<li>HMG, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/3-hydroxy-3-methylglutaryl-coa-lyase-deficiency/">3-hydroxy-3-methylglutaryl-CoA lyase deficiency</a></li>
|
||
|
||
|
||
<li>HMG-CoA lyase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/3-hydroxy-3-methylglutaryl-coa-lyase-deficiency/">3-hydroxy-3-methylglutaryl-CoA lyase deficiency</a></li>
|
||
|
||
|
||
<li>HML, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/myopathy-with-deficiency-of-iron-sulfur-cluster-assembly-enzyme/">Myopathy with deficiency of iron-sulfur cluster assembly enzyme</a></li>
|
||
|
||
|
||
<li>HMN V, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/distal-hereditary-motor-neuropathy-type-v/">Distal hereditary motor neuropathy, type V</a></li>
|
||
|
||
|
||
<li>HMN6, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/spinal-muscular-atrophy-with-respiratory-distress-type-1/">Spinal muscular atrophy with respiratory distress type 1</a></li>
|
||
|
||
|
||
<li>HMNDYT, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypermanganesemia-with-dystonia/">Hypermanganesemia with dystonia</a></li>
|
||
|
||
|
||
<li>HMNVI, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/spinal-muscular-atrophy-with-respiratory-distress-type-1/">Spinal muscular atrophy with respiratory distress type 1</a></li>
|
||
|
||
|
||
<li>HMSN, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/charcot-marie-tooth-disease/">Charcot-Marie-Tooth disease</a></li>
|
||
|
||
|
||
<li>HMSN IV, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/refsum-disease/">Refsum disease</a></li>
|
||
|
||
|
||
<li>HMSN type IV, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/refsum-disease/">Refsum disease</a></li>
|
||
|
||
|
||
<li>HMSN/ACC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/andermann-syndrome/">Andermann syndrome</a></li>
|
||
|
||
|
||
<li>HNA, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-neuralgic-amyotrophy/">Hereditary neuralgic amyotrophy</a></li>
|
||
|
||
|
||
<li>HNFJ1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/autosomal-dominant-tubulointerstitial-kidney-disease-umod/">Autosomal dominant tubulointerstitial kidney disease-UMOD</a></li>
|
||
|
||
|
||
<li>HNPCC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lynch-syndrome/">Lynch syndrome</a></li>
|
||
|
||
|
||
<li>HNPP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-neuropathy-with-liability-to-pressure-palsies/">Hereditary neuropathy with liability to pressure palsies</a></li>
|
||
|
||
|
||
<li>HNSCC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/head-and-neck-squamous-cell-carcinoma/">Head and neck squamous cell carcinoma</a></li>
|
||
|
||
|
||
<li>HOGA, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/gyrate-atrophy-of-the-choroid-and-retina/">Gyrate atrophy of the choroid and retina</a></li>
|
||
|
||
|
||
<li>HOKPP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypokalemic-periodic-paralysis/">Hypokalemic periodic paralysis</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/holocarboxylase-synthetase-deficiency/">Holocarboxylase synthetase deficiency</a></li>
|
||
|
||
<li>Holoprosencephaly and split hand/foot syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hartsfield-syndrome/">Hartsfield syndrome</a></li>
|
||
|
||
|
||
<li>Holoprosencephaly sequence, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/nonsyndromic-holoprosencephaly/">Nonsyndromic holoprosencephaly</a></li>
|
||
|
||
|
||
<li>Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hartsfield-syndrome/">Hartsfield syndrome</a></li>
|
||
|
||
|
||
<li>Holoprosencephaly, hypertelorism, and ectrodactyly syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hartsfield-syndrome/">Hartsfield syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/holt-oram-syndrome/">Holt-Oram syndrome</a></li>
|
||
|
||
<li>HOMG, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypomagnesemia-with-secondary-hypocalcemia/">Hypomagnesemia with secondary hypocalcemia</a></li>
|
||
|
||
|
||
<li>Homocysteinemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/homocystinuria/">Homocystinuria</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/homocystinuria/">Homocystinuria</a></li>
|
||
|
||
<li>Homogentisic acid oxidase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alkaptonuria/">Alkaptonuria</a></li>
|
||
|
||
|
||
<li>Homogentisic acidura, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alkaptonuria/">Alkaptonuria</a></li>
|
||
|
||
|
||
<li>Homozygous PAI-1 deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/complete-plasminogen-activator-inhibitor-1-deficiency/">Complete plasminogen activator inhibitor 1 deficiency</a></li>
|
||
|
||
|
||
<li>Honeycomb myocardium, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/left-ventricular-noncompaction/">Left ventricular noncompaction</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/horizontal-gaze-palsy-with-progressive-scoliosis/">Horizontal gaze palsy with progressive scoliosis</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/horner-syndrome/">Horner syndrome</a></li>
|
||
|
||
<li>Horner's syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/horner-syndrome/">Horner syndrome</a></li>
|
||
|
||
|
||
<li>Hornstein-Birt-Hogg-Dubé syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/birt-hogg-dube-syndrome/">Birt-Hogg-Dubé syndrome</a></li>
|
||
|
||
|
||
<li>Hornstein-Knickenberg syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/birt-hogg-dube-syndrome/">Birt-Hogg-Dubé syndrome</a></li>
|
||
|
||
|
||
<li>HOS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/holt-oram-syndrome/">Holt-Oram syndrome</a></li>
|
||
|
||
|
||
<li>HP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-pancreatitis/">Hereditary pancreatitis</a></li>
|
||
|
||
|
||
<li>HPLH, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hemophagocytic-lymphohistiocytosis/">Familial hemophagocytic lymphohistiocytosis</a></li>
|
||
|
||
|
||
<li>HPS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hermansky-pudlak-syndrome/">Hermansky-Pudlak syndrome</a></li>
|
||
|
||
|
||
<li>HPT-JT, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperparathyroidism-jaw-tumor-syndrome/">Hyperparathyroidism-jaw tumor syndrome</a></li>
|
||
|
||
|
||
<li>HS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-spherocytosis/">Hereditary spherocytosis</a></li>
|
||
|
||
|
||
<li>HSAN IA, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-neuropathy-type-ia/">Hereditary sensory neuropathy type IA</a></li>
|
||
|
||
|
||
<li>HSAN type II, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ii/">Hereditary sensory and autonomic neuropathy type II</a></li>
|
||
|
||
|
||
<li>HSAN type III, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-dysautonomia/">Familial dysautonomia</a></li>
|
||
|
||
|
||
<li>HSAN type IV, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/congenital-insensitivity-to-pain-with-anhidrosis/">Congenital insensitivity to pain with anhidrosis</a></li>
|
||
|
||
|
||
<li>HSAN type V, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-v/">Hereditary sensory and autonomic neuropathy type V</a></li>
|
||
|
||
|
||
<li>HSAN V, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-v/">Hereditary sensory and autonomic neuropathy type V</a></li>
|
||
|
||
|
||
<li>HSAN1A, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-neuropathy-type-ia/">Hereditary sensory neuropathy type IA</a></li>
|
||
|
||
|
||
<li>HSAN1E, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ie/">Hereditary sensory and autonomic neuropathy type IE</a></li>
|
||
|
||
|
||
<li>HSAN2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ii/">Hereditary sensory and autonomic neuropathy type II</a></li>
|
||
|
||
|
||
<li>HSAN2A, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ii/">Hereditary sensory and autonomic neuropathy type II</a></li>
|
||
|
||
|
||
<li>HSAN2B, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ii/">Hereditary sensory and autonomic neuropathy type II</a></li>
|
||
|
||
|
||
<li>HSAN2C, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ii/">Hereditary sensory and autonomic neuropathy type II</a></li>
|
||
|
||
|
||
<li>HSAN2D, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ii/">Hereditary sensory and autonomic neuropathy type II</a></li>
|
||
|
||
|
||
<li>HSAN3, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-dysautonomia/">Familial dysautonomia</a></li>
|
||
|
||
|
||
<li>HSAN4, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/congenital-insensitivity-to-pain-with-anhidrosis/">Congenital insensitivity to pain with anhidrosis</a></li>
|
||
|
||
|
||
<li>HSAN5, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-v/">Hereditary sensory and autonomic neuropathy type V</a></li>
|
||
|
||
|
||
<li>HSANII, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ii/">Hereditary sensory and autonomic neuropathy type II</a></li>
|
||
|
||
|
||
<li>HSCR, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hirschsprung-disease/">Hirschsprung disease</a></li>
|
||
|
||
|
||
<li>HSD10 deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hsd10-disease/">HSD10 disease</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hsd10-disease/">HSD10 disease</a></li>
|
||
|
||
<li>HSH, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypomagnesemia-with-secondary-hypocalcemia/">Hypomagnesemia with secondary hypocalcemia</a></li>
|
||
|
||
|
||
<li>HSN IA, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-neuropathy-type-ia/">Hereditary sensory neuropathy type IA</a></li>
|
||
|
||
|
||
<li>HSN IE, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ie/">Hereditary sensory and autonomic neuropathy type IE</a></li>
|
||
|
||
|
||
<li>HSN type II, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ii/">Hereditary sensory and autonomic neuropathy type II</a></li>
|
||
|
||
|
||
<li>HSN-III, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-dysautonomia/">Familial dysautonomia</a></li>
|
||
|
||
|
||
<li>HSN1A, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-neuropathy-type-ia/">Hereditary sensory neuropathy type IA</a></li>
|
||
|
||
|
||
<li>HSNIE, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-sensory-and-autonomic-neuropathy-type-ie/">Hereditary sensory and autonomic neuropathy type IE</a></li>
|
||
|
||
|
||
<li>HSP-TCC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-11/">Spastic paraplegia type 11</a></li>
|
||
|
||
|
||
<li>HTL, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/autosomal-recessive-hypotrichosis/">Autosomal recessive hypotrichosis</a></li>
|
||
|
||
|
||
<li>HTX, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/heterotaxy-syndrome/">Heterotaxy syndrome</a></li>
|
||
|
||
|
||
<li>Hughes syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/antiphospholipid-syndrome/">Antiphospholipid syndrome</a></li>
|
||
|
||
|
||
<li>Humero-spinal dysostosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/chst3-related-skeletal-dysplasia/">CHST3-related skeletal dysplasia</a></li>
|
||
|
||
|
||
<li>Hunter syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mucopolysaccharidosis-type-ii/">Mucopolysaccharidosis type II</a></li>
|
||
|
||
|
||
<li>Huntington chorea, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/huntingtons-disease/">Huntington's disease</a></li>
|
||
|
||
|
||
<li>Huntington chronic progressive hereditary chorea, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/huntingtons-disease/">Huntington's disease</a></li>
|
||
|
||
|
||
<li>Huntington disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/huntingtons-disease/">Huntington's disease</a></li>
|
||
|
||
|
||
<li>Huntington disease-like syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/huntingtons-disease-like/">Huntington's disease-like</a></li>
|
||
|
||
|
||
<li>Huntington disease-like syndromes, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/huntingtons-disease-like/">Huntington's disease-like</a></li>
|
||
|
||
|
||
<li>Huntington's chorea, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/huntingtons-disease/">Huntington's disease</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/huntingtons-disease/">Huntington's disease</a></li>
|
||
|
||
<li>Huntington's disease phenocopies, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/huntingtons-disease-like/">Huntington's disease-like</a></li>
|
||
|
||
|
||
<li>Huntington's disease phenocopy syndromes, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/huntingtons-disease-like/">Huntington's disease-like</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/huntingtons-disease-like/">Huntington's disease-like</a></li>
|
||
|
||
<li>Huntington's disease-like syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/huntingtons-disease-like/">Huntington's disease-like</a></li>
|
||
|
||
|
||
<li>Huntington's disease-like syndromes, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/huntingtons-disease-like/">Huntington's disease-like</a></li>
|
||
|
||
|
||
<li>Hurler syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mucopolysaccharidosis-type-i/">Mucopolysaccharidosis type I</a></li>
|
||
|
||
|
||
<li>Hurler-Scheie syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mucopolysaccharidosis-type-i/">Mucopolysaccharidosis type I</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hutchinson-gilford-progeria-syndrome/">Hutchinson-Gilford progeria syndrome</a></li>
|
||
|
||
<li>Hutchinson-Gilford syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hutchinson-gilford-progeria-syndrome/">Hutchinson-Gilford progeria syndrome</a></li>
|
||
|
||
|
||
<li>Hutterite syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/bowen-conradi-syndrome/">Bowen-Conradi syndrome</a></li>
|
||
|
||
|
||
<li>HV, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/bunion/">Bunion</a></li>
|
||
|
||
|
||
<li>HVDAS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/adnp-syndrome/">ADNP syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hyaline-fibromatosis-syndrome/">Hyaline fibromatosis syndrome</a></li>
|
||
|
||
<li>Hyalinosis cutis et mucosae, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lipoid-proteinosis/">Lipoid proteinosis</a></li>
|
||
|
||
|
||
<li>Hyaloideoretinal degeneration of Wagner, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/wagner-syndrome/">Wagner syndrome</a></li>
|
||
|
||
|
||
<li>Hydrocephalus, agyria, and retinal dysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/walker-warburg-syndrome/">Walker-Warburg syndrome</a></li>
|
||
|
||
|
||
<li>Hydrocephalus, internal, Dandy-Walker type, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dandy-walker-malformation/">Dandy-Walker malformation</a></li>
|
||
|
||
|
||
<li>Hydrocephalus, noncommunicating, Dandy-Walker type, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dandy-walker-malformation/">Dandy-Walker malformation</a></li>
|
||
|
||
|
||
<li>Hydrometrocolpos syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mckusick-kaufman-syndrome/">McKusick-Kaufman syndrome</a></li>
|
||
|
||
|
||
<li>Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mckusick-kaufman-syndrome/">McKusick-Kaufman syndrome</a></li>
|
||
|
||
|
||
<li>Hydrometrocolpos-postaxial polydactyly syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mckusick-kaufman-syndrome/">McKusick-Kaufman syndrome</a></li>
|
||
|
||
|
||
<li>Hydronephrosis with peculiar facial expression, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ochoa-syndrome/">Ochoa syndrome</a></li>
|
||
|
||
|
||
<li>Hydronephrosis-inverted smile, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ochoa-syndrome/">Ochoa syndrome</a></li>
|
||
|
||
|
||
<li>Hydrops - ectopic calcification - moth-eaten skeletal dysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/greenberg-dysplasia/">Greenberg dysplasia</a></li>
|
||
|
||
|
||
<li>Hydroxyacyl-CoA dehydrogenase II deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hsd10-disease/">HSD10 disease</a></li>
|
||
|
||
|
||
<li>Hydroxymethylglutaric aciduria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/3-hydroxy-3-methylglutaryl-coa-lyase-deficiency/">3-hydroxy-3-methylglutaryl-CoA lyase deficiency</a></li>
|
||
|
||
|
||
<li>Hyper IgD syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mevalonate-kinase-deficiency/">Mevalonate kinase deficiency</a></li>
|
||
|
||
|
||
<li>Hyper IgE recurrent infection syndrome, autosomal recessive, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dock8-immunodeficiency-syndrome/">DOCK8 immunodeficiency syndrome</a></li>
|
||
|
||
|
||
<li>Hyper immunoglobulin E syndrome, autosomal recessive, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dock8-immunodeficiency-syndrome/">DOCK8 immunodeficiency syndrome</a></li>
|
||
|
||
|
||
<li>Hyper-IgM immunodeficiency with hypohidrotic ectodermal dysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/anhidrotic-ectodermal-dysplasia-with-immune-deficiency/">Anhidrotic ectodermal dysplasia with immune deficiency</a></li>
|
||
|
||
|
||
<li>Hyper-IgM syndrome 1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/x-linked-hyper-igm-syndrome/">X-linked hyper IgM syndrome</a></li>
|
||
|
||
|
||
<li>Hyperaldosteronism, familial, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hyperaldosteronism/">Familial hyperaldosteronism</a></li>
|
||
|
||
|
||
<li>Hyperammonemia due to carbonic anhydrase VA deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/carbonic-anhydrase-va-deficiency/">Carbonic anhydrase VA deficiency</a></li>
|
||
|
||
|
||
<li>Hyperammonemia, type III, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/n-acetylglutamate-synthase-deficiency/">N-acetylglutamate synthase deficiency</a></li>
|
||
|
||
|
||
<li>Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/carbonic-anhydrase-va-deficiency/">Carbonic anhydrase VA deficiency</a></li>
|
||
|
||
|
||
<li>Hyperargininemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/arginase-deficiency/">Arginase deficiency</a></li>
|
||
|
||
|
||
<li>Hyperbilirubinemia 1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/gilbert-syndrome/">Gilbert syndrome</a></li>
|
||
|
||
|
||
<li>Hyperbilirubinemia II, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dubin-johnson-syndrome/">Dubin-Johnson syndrome</a></li>
|
||
|
||
|
||
<li>Hyperbilirubinemia, Dubin-Johnson type, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dubin-johnson-syndrome/">Dubin-Johnson syndrome</a></li>
|
||
|
||
|
||
<li>Hyperbilirubinemia, Rotor type, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/rotor-syndrome/">Rotor syndrome</a></li>
|
||
|
||
|
||
<li>Hypercalcemia-supravalvar aortic stenosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/williams-syndrome/">Williams syndrome</a></li>
|
||
|
||
|
||
<li>Hypercortisolism, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cushing-disease/">Cushing disease</a></li>
|
||
|
||
|
||
<li>Hyperdibasic aminoaciduria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lysinuric-protein-intolerance/">Lysinuric protein intolerance</a></li>
|
||
|
||
|
||
<li>Hyperekplexia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hyperekplexia/">Hereditary hyperekplexia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hyperferritinemia-cataract-syndrome/">Hyperferritinemia-cataract syndrome</a></li>
|
||
|
||
<li>Hyperfibrinolysis due to PAI1 deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/complete-plasminogen-activator-inhibitor-1-deficiency/">Complete plasminogen activator inhibitor 1 deficiency</a></li>
|
||
|
||
|
||
<li>Hyperglycinemia with ketoacidosis and leukopenia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/propionic-acidemia/">Propionic acidemia</a></li>
|
||
|
||
|
||
<li>Hyperhistidinemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/histidinemia/">Histidinemia</a></li>
|
||
|
||
|
||
<li>Hyperimidodipeptiduria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/prolidase-deficiency/">Prolidase deficiency</a></li>
|
||
|
||
|
||
<li>Hyperimmunoglobulin D with periodic fever, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mevalonate-kinase-deficiency/">Mevalonate kinase deficiency</a></li>
|
||
|
||
|
||
<li>Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dock8-immunodeficiency-syndrome/">DOCK8 immunodeficiency syndrome</a></li>
|
||
|
||
|
||
<li>Hyperimmunoglobulin E syndrome type 2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dock8-immunodeficiency-syndrome/">DOCK8 immunodeficiency syndrome</a></li>
|
||
|
||
|
||
<li>Hyperimmunoglobulinemia D, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mevalonate-kinase-deficiency/">Mevalonate kinase deficiency</a></li>
|
||
|
||
|
||
<li>Hyperinsulinemia hypoglycemia of infancy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/congenital-hyperinsulinism/">Congenital hyperinsulinism</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hyperkalemic-periodic-paralysis/">Hyperkalemic periodic paralysis</a></li>
|
||
|
||
<li>Hyperkeratosis, epidermolytic, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/epidermolytic-hyperkeratosis/">Epidermolytic hyperkeratosis</a></li>
|
||
|
||
|
||
<li>Hyperkinetic disorder, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/attention-deficit-hyperactivity-disorder/">Attention-deficit/hyperactivity disorder</a></li>
|
||
|
||
|
||
<li>Hyperkinetic syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/attention-deficit-hyperactivity-disorder/">Attention-deficit/hyperactivity disorder</a></li>
|
||
|
||
|
||
<li>HyperKPP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperkalemic-periodic-paralysis/">Hyperkalemic periodic paralysis</a></li>
|
||
|
||
|
||
<li>Hyperlipidemia due to hepatic triglyceride lipase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hepatic-lipase-deficiency/">Hepatic lipase deficiency</a></li>
|
||
|
||
|
||
<li>Hyperlipoproteinemia type I, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-lipoprotein-lipase-deficiency/">Familial lipoprotein lipase deficiency</a></li>
|
||
|
||
|
||
<li>Hyperlipoproteinemia type Ia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-lipoprotein-lipase-deficiency/">Familial lipoprotein lipase deficiency</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hyperlysinemia/">Hyperlysinemia</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hypermanganesemia-with-dystonia/">Hypermanganesemia with dystonia</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hypermethioninemia/">Hypermethioninemia</a></li>
|
||
|
||
<li>Hypermetropia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/farsightedness/">Farsightedness</a></li>
|
||
|
||
|
||
<li>Hyperopia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/farsightedness/">Farsightedness</a></li>
|
||
|
||
|
||
<li>Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ornithine-translocase-deficiency/">Ornithine translocase deficiency</a></li>
|
||
|
||
|
||
<li>Hyperornithinemia with gyrate atrophy of choroid and retina, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/gyrate-atrophy-of-the-choroid-and-retina/">Gyrate atrophy of the choroid and retina</a></li>
|
||
|
||
|
||
<li>Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ornithine-translocase-deficiency/">Ornithine translocase deficiency</a></li>
|
||
|
||
|
||
<li>Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ornithine-translocase-deficiency/">Ornithine translocase deficiency</a></li>
|
||
|
||
|
||
<li>Hyperostosis corticalis deformans juvenilis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/juvenile-paget-disease/">Juvenile Paget disease</a></li>
|
||
|
||
|
||
<li>Hyperostosis corticalis generalisata, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/sost-related-sclerosing-bone-dysplasia/">SOST-related sclerosing bone dysplasia</a></li>
|
||
|
||
|
||
<li>Hyperostosis, monomelic, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/melorheostosis/">Melorheostosis</a></li>
|
||
|
||
|
||
<li>Hyperotosis corticalis generalisata familiaris, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/sost-related-sclerosing-bone-dysplasia/">SOST-related sclerosing bone dysplasia</a></li>
|
||
|
||
|
||
<li>Hyperoxaluria, primary, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/primary-hyperoxaluria/">Primary hyperoxaluria</a></li>
|
||
|
||
|
||
<li>Hyperparathyroidism 1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-isolated-hyperparathyroidism/">Familial isolated hyperparathyroidism</a></li>
|
||
|
||
|
||
<li>Hyperparathyroidism 2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperparathyroidism-jaw-tumor-syndrome/">Hyperparathyroidism-jaw tumor syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hyperparathyroidism-jaw-tumor-syndrome/">Hyperparathyroidism-jaw tumor syndrome</a></li>
|
||
|
||
<li>Hyperphenylalaninemia caused by a defect in biopterin metabolism, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tetrahydrobiopterin-deficiency/">Tetrahydrobiopterin deficiency</a></li>
|
||
|
||
|
||
<li>Hyperphenylalaninemia, non-phenylketonuric, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tetrahydrobiopterin-deficiency/">Tetrahydrobiopterin deficiency</a></li>
|
||
|
||
|
||
<li>Hyperphosphatasemia tarda, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/sost-related-sclerosing-bone-dysplasia/">SOST-related sclerosing bone dysplasia</a></li>
|
||
|
||
|
||
<li>Hyperphosphatasemia with bone disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/juvenile-paget-disease/">Juvenile Paget disease</a></li>
|
||
|
||
|
||
<li>Hyperphosphatasia with mental retardation syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mabry-syndrome/">Mabry syndrome</a></li>
|
||
|
||
|
||
<li>Hyperphosphatasia with seizures and neurologic deficit, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mabry-syndrome/">Mabry syndrome</a></li>
|
||
|
||
|
||
<li>Hyperphosphatasia, familial idiopathic, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/juvenile-paget-disease/">Juvenile Paget disease</a></li>
|
||
|
||
|
||
<li>Hyperphosphatemia hyperostosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperphosphatemic-familial-tumoral-calcinosis/">Hyperphosphatemic familial tumoral calcinosis</a></li>
|
||
|
||
|
||
<li>Hyperphosphatemia hyperostosis syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperphosphatemic-familial-tumoral-calcinosis/">Hyperphosphatemic familial tumoral calcinosis</a></li>
|
||
|
||
|
||
<li>Hyperphosphatemia tumoral calcinosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperphosphatemic-familial-tumoral-calcinosis/">Hyperphosphatemic familial tumoral calcinosis</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hyperphosphatemic-familial-tumoral-calcinosis/">Hyperphosphatemic familial tumoral calcinosis</a></li>
|
||
|
||
<li>HyperPP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperkalemic-periodic-paralysis/">Hyperkalemic periodic paralysis</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hyperprolinemia/">Hyperprolinemia</a></li>
|
||
|
||
<li>Hyperpyrexia, malignant, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/malignant-hyperthermia/">Malignant hyperthermia</a></li>
|
||
|
||
|
||
<li>Hypertelorism with esophageal abnormalities and hypospadias, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/opitz-g-bbb-syndrome/">Opitz G/BBB syndrome</a></li>
|
||
|
||
|
||
<li>Hypertelorism-hypospadias sydrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/opitz-g-bbb-syndrome/">Opitz G/BBB syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hypertension/">Hypertension</a></li>
|
||
|
||
<li>Hyperthermia, malignant, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/malignant-hyperthermia/">Malignant hyperthermia</a></li>
|
||
|
||
|
||
<li>Hypertrabeculation syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/left-ventricular-noncompaction/">Left ventricular noncompaction</a></li>
|
||
|
||
|
||
<li>Hypertrichosis-osteochondrodysplasia-cardiomegaly syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cantu-syndrome/">Cantú syndrome</a></li>
|
||
|
||
|
||
<li>Hypertrichotic osteochondrodysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cantu-syndrome/">Cantú syndrome</a></li>
|
||
|
||
|
||
<li>Hypertrophic arthritis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/osteoarthritis/">Osteoarthritis</a></li>
|
||
|
||
|
||
<li>Hypertyrosinaemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tyrosinemia/">Tyrosinemia</a></li>
|
||
|
||
|
||
<li>Hypertyrosinemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tyrosinemia/">Tyrosinemia</a></li>
|
||
|
||
|
||
<li>Hypobetalipoproteinemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hypobetalipoproteinemia/">Familial hypobetalipoproteinemia</a></li>
|
||
|
||
|
||
<li>Hypobetalipoproteinemia with accumulation of apolipoprotein B-like protein in intestinal cells, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/chylomicron-retention-disease/">Chylomicron retention disease</a></li>
|
||
|
||
|
||
<li>Hypoceruloplasminemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/aceruloplasminemia/">Aceruloplasminemia</a></li>
|
||
|
||
|
||
<li>Hypochondrodysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypochondroplasia/">Hypochondroplasia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hypochondroplasia/">Hypochondroplasia</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hypochromic-microcytic-anemia-with-iron-overload/">Hypochromic microcytic anemia with iron overload</a></li>
|
||
|
||
<li>Hypocupremia, congenital, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/menkes-syndrome/">Menkes syndrome</a></li>
|
||
|
||
|
||
<li>Hypogammaglobulinemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/x-linked-agammaglobulinemia/">X-linked agammaglobulinemia</a></li>
|
||
|
||
|
||
<li>Hypoglycemia with deficiency of glycogen synthetase, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glycogen-storage-disease-type-0/">Glycogen storage disease type 0</a></li>
|
||
|
||
|
||
<li>Hypogonadism with anosmia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/kallmann-syndrome/">Kallmann syndrome</a></li>
|
||
|
||
|
||
<li>Hypogonadotropic hypogonadism and anosmia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/kallmann-syndrome/">Kallmann syndrome</a></li>
|
||
|
||
|
||
<li>Hypogonadotropic hypogonadism-anosmia syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/kallmann-syndrome/">Kallmann syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hypohidrotic-ectodermal-dysplasia/">Hypohidrotic ectodermal dysplasia</a></li>
|
||
|
||
<li>Hypohidrotic ectodermal dysplasia with immune deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/anhidrotic-ectodermal-dysplasia-with-immune-deficiency/">Anhidrotic ectodermal dysplasia with immune deficiency</a></li>
|
||
|
||
|
||
<li>Hypokalemia-hypomagnesemia, primary renotubular, with hypocalciuria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/gitelman-syndrome/">Gitelman syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hypokalemic-periodic-paralysis/">Hypokalemic periodic paralysis</a></li>
|
||
|
||
<li>HypoKPP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypokalemic-periodic-paralysis/">Hypokalemic periodic paralysis</a></li>
|
||
|
||
|
||
<li>Hypolactasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lactose-intolerance/">Lactose intolerance</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hypomagnesemia-with-secondary-hypocalcemia/">Hypomagnesemia with secondary hypocalcemia</a></li>
|
||
|
||
<li>Hypomagnesemic tetany, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypomagnesemia-with-secondary-hypocalcemia/">Hypomagnesemia with secondary hypocalcemia</a></li>
|
||
|
||
|
||
<li>Hypomelia hypotrichosis facial hemangioma syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/roberts-syndrome/">Roberts syndrome</a></li>
|
||
|
||
|
||
<li>Hypomyelinating leukodystrophy 2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pelizaeus-merzbacher-like-disease-type-1/">Pelizaeus-Merzbacher-like disease type 1</a></li>
|
||
|
||
|
||
<li>Hypomyelinating leukodystrophy, 1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pelizaeus-merzbacher-disease/">Pelizaeus-Merzbacher disease</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hypomyelination-and-congenital-cataract/">Hypomyelination and congenital cataract</a></li>
|
||
|
||
<li>Hypomyelination with brain stem and spinal cord involvement and leg spasticity, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypomyelination-with-brainstem-and-spinal-cord-involvement-and-leg-spasticity/">Hypomyelination with brainstem and spinal cord involvement and leg spasticity</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hypomyelination-with-brainstem-and-spinal-cord-involvement-and-leg-spasticity/">Hypomyelination with brainstem and spinal cord involvement and leg spasticity</a></li>
|
||
|
||
<li>Hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pol-iii-related-leukodystrophy/">Pol III-related leukodystrophy</a></li>
|
||
|
||
|
||
<li>Hypomyelination, hypodontia, hypogonadotropic hypogonadism, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pol-iii-related-leukodystrophy/">Pol III-related leukodystrophy</a></li>
|
||
|
||
|
||
<li>Hyponychia congenita, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/anonychia-congenita/">Anonychia congenita</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hypophosphatasia/">Hypophosphatasia</a></li>
|
||
|
||
<li>Hypophosphatemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hypophosphatemic-rickets/">Hereditary hypophosphatemic rickets</a></li>
|
||
|
||
|
||
<li>Hypopigmentation immunodeficiency disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/griscelli-syndrome/">Griscelli syndrome</a></li>
|
||
|
||
|
||
<li>Hypopigmentation-deafness syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tietz-syndrome/">Tietz syndrome</a></li>
|
||
|
||
|
||
<li>Hypopigmentation/deafness of Tietz, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tietz-syndrome/">Tietz syndrome</a></li>
|
||
|
||
|
||
<li>Hypoplasia of spleen, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/isolated-congenital-asplenia/">Isolated congenital asplenia</a></li>
|
||
|
||
|
||
<li>Hypoplasminogenemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/congenital-plasminogen-deficiency/">Congenital plasminogen deficiency</a></li>
|
||
|
||
|
||
<li>Hypoplastic congenital anemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/diamond-blackfan-anemia/">Diamond-Blackfan anemia</a></li>
|
||
|
||
|
||
<li>HypoPP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypokalemic-periodic-paralysis/">Hypokalemic periodic paralysis</a></li>
|
||
|
||
|
||
<li>Hypoproconvertinemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/factor-vii-deficiency/">Factor VII deficiency</a></li>
|
||
|
||
|
||
<li>Hypoprothrombinemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/prothrombin-deficiency/">Prothrombin deficiency</a></li>
|
||
|
||
|
||
<li>Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/bosma-arhinia-microphthalmia-syndrome/">Bosma arhinia microphthalmia syndrome</a></li>
|
||
|
||
|
||
<li>Hypospadias-dysphagia syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/opitz-g-bbb-syndrome/">Opitz G/BBB syndrome</a></li>
|
||
|
||
|
||
<li>Hyposplenia, isolated congenital, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/isolated-congenital-asplenia/">Isolated congenital asplenia</a></li>
|
||
|
||
|
||
<li>Hypotension, orthostatic, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/orthostatic-hypotension/">Orthostatic hypotension</a></li>
|
||
|
||
|
||
<li>Hypotension, postural, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/orthostatic-hypotension/">Orthostatic hypotension</a></li>
|
||
|
||
|
||
<li>Hypotonia, obesity, and prominent incisors, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cohen-syndrome/">Cohen syndrome</a></li>
|
||
|
||
|
||
<li>Hypotrichoses, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/autosomal-recessive-hypotrichosis/">Autosomal recessive hypotrichosis</a></li>
|
||
|
||
|
||
<li>Hypotrichosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/autosomal-recessive-hypotrichosis/">Autosomal recessive hypotrichosis</a></li>
|
||
|
||
|
||
<li>Hypoxanthine guanine phosphoribosyltransferase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lesch-nyhan-syndrome/">Lesch-Nyhan syndrome</a></li>
|
||
|
||
|
||
<li>Hypoxanthine phosphoribosyltransferase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lesch-nyhan-syndrome/">Lesch-Nyhan syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/hystrix-like-ichthyosis-with-deafness/">Hystrix-like ichthyosis with deafness</a></li>
|
||
|
||
</ul>
|
||
|
||
</section>
|
||
|
||
<section>
|
||
<!--
|
||
<div class="from-ghr">
|
||
<img src="https://medlineplus.gov/images/fromGHR.png" alt="From Genetics Home Reference" />
|
||
<p>Genetics Home Reference has merged with MedlinePlus. Genetics Home Reference content now can be found in the "Genetics" section of MedlinePlus. <a href="https://medlineplus.gov/about/general/genetics/newhome/">Learn more</a></p>
|
||
</div>
|
||
-->
|
||
|
||
|
||
</section>
|
||
|
||
</div>
|
||
</article>
|
||
|
||
</div>
|
||
|
||
|
||
</div>
|
||
|
||
<footer>
|
||
<div id="mplus-footer">
|
||
<div class="footer1">
|
||
|
||
<ul class="secondarynav">
|
||
<li><a href="https://medlineplus.gov/about/">About MedlinePlus</a></li>
|
||
<li><a href="https://medlineplus.gov/whatsnew/">What's New</a></li>
|
||
<li><a href="https://medlineplus.gov/sitemap.html">Site Map</a></li>
|
||
|
||
|
||
<li><a href="https://support.nlm.nih.gov/knowledgebase/category/?id=CAT-01231&category=medlineplus&from=https%3A//medlineplus.gov/genetics/condition-h/" target="_blank"><span>Customer Support</span></a></li>
|
||
|
||
</ul>
|
||
|
||
<ul class="follow-footer">
|
||
<li>
|
||
<a href="https://medlineplus.gov/rss.html" class="follow-item">Subscribe to RSS<img src="https://medlineplus.gov/images/feed.png" class="social-media-toolkit-icon" alt="RSS" title="RSS"></a>
|
||
</li>
|
||
<li>
|
||
<span class="follow-label">Follow us</span>
|
||
<a href="https://twitter.com/medlineplus" class="follow-item" target="_blank">
|
||
<img src="https://medlineplus.gov/images/i_share_twitter.png" class="follow-icon" alt="X" title="X">
|
||
</a>
|
||
<a href="https://facebook.com/Mplus.gov/" class="follow-item" target="_blank">
|
||
<img src="https://medlineplus.gov/images/i_share_fb.png" class="follow-icon" alt="Facebook" title="Facebook">
|
||
</a>
|
||
<a href="https://www.instagram.com/mplusgov/" class="follow-item" target="_blank">
|
||
<img src="https://medlineplus.gov/images/Instagram_Glyph_Gradient_RGB.png" class="follow-icon" alt="Instagram" title="Instagram">
|
||
</a>
|
||
</li>
|
||
<li>
|
||
<a href="https://medlineplus.gov/social-media-toolkit/" class="social-media-toolkit-item">Social Media Toolkit<img src="https://medlineplus.gov/images/i_social_media_toolkit.png" class="social-media-toolkit-icon" alt="Social Media Toolkit" title="Social Media Toolkit"></a>
|
||
</li>
|
||
</ul>
|
||
</div>
|
||
|
||
<div class="footer2">
|
||
<ul>
|
||
|
||
|
||
<li><a href=" https://www.nlm.nih.gov/web_policies.html" target='_blank'>NLM Web Policies</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/about/using/usingcontent/" >Copyright</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/accessibility.html">Accessibility</a></li>
|
||
<li><a href="https://medlineplus.gov/about/using/criteria/">Guidelines for Links</a></li>
|
||
<li><a href="https://medlineplus.gov/plugins.html">Viewers & Players</a></li>
|
||
<li><a href="https://www.hhs.gov/vulnerability-disclosure-policy/index.html" target="_blank">HHS Vulnerability Disclosure</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/medlineplus-connect/">MedlinePlus Connect for EHRs</a></li>
|
||
<li><a href="https://medlineplus.gov/about/developers/">For Developers</a></li>
|
||
|
||
</ul>
|
||
|
||
<div class="address">
|
||
<a href="https://www.nlm.nih.gov" target="_blank">National Library of Medicine</a>
|
||
<span>8600 Rockville Pike, Bethesda, MD 20894</span>
|
||
<a href="https://www.hhs.gov" target="_blank">U.S. Department of Health and Human Services</a>
|
||
<a href="https://www.nih.gov" target="_blank">National Institutes of Health</a>
|
||
|
||
</div>
|
||
|
||
|
||
<div class="date">
|
||
|
||
|
||
|
||
|
||
|
||
</div>
|
||
|
||
|
||
<div class="return-top"><a href="#top" title="Return to top"><img class="return-top-icon" alt="Return to top" src="https://medlineplus.gov/images/return-top.png"></a></div>
|
||
</div>
|
||
</div>
|
||
</footer>
|
||
</div>
|
||
|
||
|
||
<script src="https://medlineplus.gov/jslib/jquery-3.6.0.min.js" type="text/javascript"></script>
|
||
<script src="https://medlineplus.gov/jslib/mplus-frontend-controls-new.js" type="text/javascript"></script>
|
||
<script src="https://medlineplus.gov/jslib/mplus-share.js?id=1112022" type="text/javascript"></script>
|
||
<!--[if lte IE 9]><script src="//www.nlm.nih.gov/medlineplus/jslib/jquery.placeholder.js" type="text/javascript"></script><![endif]-->
|
||
<script src="https://medlineplus.gov/jslib/control.js" type="text/javascript"></script>
|
||
<script src="https://medlineplus.gov/uswds/js/uswds.min.js" type="text/javascript"></script>
|
||
|
||
|
||
|
||
|
||
|
||
</body>
|
||
</html>
|