1742 lines
93 KiB
HTML
1742 lines
93 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-f/" />
|
||
|
||
|
||
|
||
|
||
<link href="https://medlineplus.gov/genetics/condition-f/" 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: F" />
|
||
<meta property="og:url" content="https://medlineplus.gov/genetics/condition-f/" />
|
||
|
||
|
||
|
||
<meta property="og:image" content="https://medlineplus.gov/images/GeneticCondition_Share.jpg" />
|
||
|
||
|
||
|
||
|
||
|
||
|
||
|
||
|
||
|
||
|
||
|
||
<title>MedlinePlus: Genetic Conditions: F</title>
|
||
|
||
<link rel="stylesheet" href="https://medlineplus.gov/css/common_new.css?1738956700649" />
|
||
<!--[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-f/" 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: F</span>
|
||
</div>
|
||
|
||
|
||
</div>
|
||
</div>
|
||
<span class="page-url print-only">URL of this page: https://medlineplus.gov/genetics/condition-f/</span>
|
||
|
||
<div >
|
||
|
||
<article>
|
||
<div class="page-info">
|
||
<div class="page-title">
|
||
<a name="start" id="start"></a>
|
||
<h1>Genetic Conditions: F</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><span class="active">F</span></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-g/" data-alpha="G">G</a></li>
|
||
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition-h/" data-alpha="H">H</a></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>F10 deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/factor-x-deficiency/">Factor X deficiency</a></li>
|
||
|
||
|
||
<li>F11 deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/factor-xi-deficiency/">Factor XI deficiency</a></li>
|
||
|
||
|
||
<li>F7 deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/factor-vii-deficiency/">Factor VII deficiency</a></li>
|
||
|
||
|
||
<li>FA, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fanconi-anemia/">Fanconi anemia</a></li>
|
||
|
||
|
||
<li>FA, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/friedreich-ataxia/">Friedreich ataxia</a></li>
|
||
|
||
|
||
<li>FAA, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-thoracic-aortic-aneurysm-and-dissection/">Familial thoracic aortic aneurysm and dissection</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fabry-disease/">Fabry disease</a></li>
|
||
|
||
<li>Fabry's disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fabry-disease/">Fabry disease</a></li>
|
||
|
||
|
||
<li>Facio-digito-genital dysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/aarskog-scott-syndrome/">Aarskog-Scott syndrome</a></li>
|
||
|
||
|
||
<li>Facio-genito-popliteal syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/popliteal-pterygium-syndrome/">Popliteal pterygium syndrome</a></li>
|
||
|
||
|
||
<li>Facio-scapulo-humeral dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/facioscapulohumeral-muscular-dystrophy/">Facioscapulohumeral muscular dystrophy</a></li>
|
||
|
||
|
||
<li>Facioauriculovertebral dysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/craniofacial-microsomia/">Craniofacial microsomia</a></li>
|
||
|
||
|
||
<li>Faciocutaneoskeletal syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/costello-syndrome/">Costello syndrome</a></li>
|
||
|
||
|
||
<li>Faciodigitogenital syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/aarskog-scott-syndrome/">Aarskog-Scott syndrome</a></li>
|
||
|
||
|
||
<li>Faciogenital dysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/aarskog-scott-syndrome/">Aarskog-Scott syndrome</a></li>
|
||
|
||
|
||
<li>Faciooculoacousticorenal syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/donnai-barrow-syndrome/">Donnai-Barrow syndrome</a></li>
|
||
|
||
|
||
<li>Faciopalatoosseous syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/otopalatodigital-syndrome-type-1/">Otopalatodigital syndrome type 1</a></li>
|
||
|
||
|
||
<li>Faciopalatoosseous syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/otopalatodigital-syndrome-type-2/">Otopalatodigital syndrome type 2</a></li>
|
||
|
||
|
||
<li>Facioscapulohumeral atrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/facioscapulohumeral-muscular-dystrophy/">Facioscapulohumeral muscular dystrophy</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/facioscapulohumeral-muscular-dystrophy/">Facioscapulohumeral muscular dystrophy</a></li>
|
||
|
||
<li>Facioscapulohumeral type progressive muscular dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/facioscapulohumeral-muscular-dystrophy/">Facioscapulohumeral muscular dystrophy</a></li>
|
||
|
||
|
||
<li>Facioscapuloperoneal muscular dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/facioscapulohumeral-muscular-dystrophy/">Facioscapulohumeral muscular dystrophy</a></li>
|
||
|
||
|
||
<li>Factor 11 deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/factor-xi-deficiency/">Factor XI deficiency</a></li>
|
||
|
||
|
||
<li>Factor II deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/prothrombin-deficiency/">Prothrombin deficiency</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/factor-v-deficiency/">Factor V deficiency</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/factor-v-leiden-thrombophilia/">Factor V Leiden thrombophilia</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/factor-vii-deficiency/">Factor VII deficiency</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/factor-x-deficiency/">Factor X deficiency</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/factor-xi-deficiency/">Factor XI deficiency</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/factor-xiii-deficiency/">Factor XIII deficiency</a></li>
|
||
|
||
<li>FACU, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/plcg2-associated-antibody-deficiency-and-immune-dysregulation/">PLCG2-associated antibody deficiency and immune dysregulation</a></li>
|
||
|
||
|
||
<li>FAHN, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fatty-acid-hydroxylase-associated-neurodegeneration/">Fatty acid hydroxylase-associated neurodegeneration</a></li>
|
||
|
||
|
||
<li>Fairbank-Keats syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/osteoglophonic-dysplasia/">Osteoglophonic dysplasia</a></li>
|
||
|
||
|
||
<li>FALDH deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/sjogren-larsson-syndrome/">Sjögren-Larsson syndrome</a></li>
|
||
|
||
|
||
<li>Familial acoustic neuromas, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/neurofibromatosis-type-2/">Neurofibromatosis type 2</a></li>
|
||
|
||
|
||
<li>Familial acute myeloid leukaemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-acute-myeloid-leukemia-with-mutated-cebpa/">Familial acute myeloid leukemia with mutated CEBPA</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-acute-myeloid-leukemia-with-mutated-cebpa/">Familial acute myeloid leukemia with mutated CEBPA</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-adenomatous-polyposis/">Familial adenomatous polyposis</a></li>
|
||
|
||
<li>Familial afibrinogenemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/congenital-afibrinogenemia/">Congenital afibrinogenemia</a></li>
|
||
|
||
|
||
<li>Familial Alzheimer disease (FAD), <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alzheimers-disease/">Alzheimer's disease</a></li>
|
||
|
||
|
||
<li>Familial amyloid polyneuropathy type IV, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lattice-corneal-dystrophy-type-ii/">Lattice corneal dystrophy type II</a></li>
|
||
|
||
|
||
<li>Familial amyloidosis, Finnish type, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lattice-corneal-dystrophy-type-ii/">Lattice corneal dystrophy type II</a></li>
|
||
|
||
|
||
<li>Familial aortic aneurysm, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-thoracic-aortic-aneurysm-and-dissection/">Familial thoracic aortic aneurysm and dissection</a></li>
|
||
|
||
|
||
<li>Familial aortic dissection, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-thoracic-aortic-aneurysm-and-dissection/">Familial thoracic aortic aneurysm and dissection</a></li>
|
||
|
||
|
||
<li>Familial aplasia of the vermis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/joubert-syndrome/">Joubert syndrome</a></li>
|
||
|
||
|
||
<li>Familial apoceruloplasmin deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/aceruloplasminemia/">Aceruloplasminemia</a></li>
|
||
|
||
|
||
<li>Familial asymmetric septal hypertrophy, <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/familial-atrial-fibrillation/">Familial atrial fibrillation</a></li>
|
||
|
||
<li>Familial atypical cold urticaria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/plcg2-associated-antibody-deficiency-and-immune-dysregulation/">PLCG2-associated antibody deficiency and immune dysregulation</a></li>
|
||
|
||
|
||
<li>Familial benign chronic pemphigus, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hailey-hailey-disease/">Hailey-Hailey disease</a></li>
|
||
|
||
|
||
<li>Familial benign giant-cell tumor of the jaw, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cherubism/">Cherubism</a></li>
|
||
|
||
|
||
<li>Familial brachial plexus neuritis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-neuralgic-amyotrophy/">Hereditary neuralgic amyotrophy</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-candidiasis/">Familial candidiasis</a></li>
|
||
|
||
<li>Familial cavernous hemangioma, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cerebral-cavernous-malformation/">Cerebral cavernous malformation</a></li>
|
||
|
||
|
||
<li>Familial cavernous malformation, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cerebral-cavernous-malformation/">Cerebral cavernous malformation</a></li>
|
||
|
||
|
||
<li>Familial cerebral cavernous angioma, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cerebral-cavernous-malformation/">Cerebral cavernous malformation</a></li>
|
||
|
||
|
||
<li>Familial cerebral cavernous malformation, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cerebral-cavernous-malformation/">Cerebral cavernous malformation</a></li>
|
||
|
||
|
||
<li>Familial chronic mucocutaneous candidiasis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-candidiasis/">Familial candidiasis</a></li>
|
||
|
||
|
||
<li>Familial cold autoinflammatory syndrome 3, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/plcg2-associated-antibody-deficiency-and-immune-dysregulation/">PLCG2-associated antibody deficiency and immune dysregulation</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-cold-autoinflammatory-syndrome-type-2/">Familial cold autoinflammatory syndrome type 2</a></li>
|
||
|
||
<li>Familial cold urticaria with common variable immunodeficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/plcg2-associated-antibody-deficiency-and-immune-dysregulation/">PLCG2-associated antibody deficiency and immune dysregulation</a></li>
|
||
|
||
|
||
<li>Familial cold-induced autoinflammatory syndrome type 2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-cold-autoinflammatory-syndrome-type-2/">Familial cold autoinflammatory syndrome type 2</a></li>
|
||
|
||
|
||
<li>Familial cystic parathyroid adenomatosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperparathyroidism-jaw-tumor-syndrome/">Hyperparathyroidism-jaw tumor syndrome</a></li>
|
||
|
||
|
||
<li>Familial dementia with neuroserpin inclusion bodies, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-encephalopathy-with-neuroserpin-inclusion-bodies/">Familial encephalopathy with neuroserpin inclusion bodies</a></li>
|
||
|
||
|
||
<li>Familial diffuse gastric cancer, <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/familial-dilated-cardiomyopathy/">Familial dilated cardiomyopathy</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-dysautonomia/">Familial dysautonomia</a></li>
|
||
|
||
<li>Familial dyskinesia with facial myokymia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/adcy5-related-dyskinesia/">ADCY5-related dyskinesia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-encephalopathy-with-neuroserpin-inclusion-bodies/">Familial encephalopathy with neuroserpin inclusion bodies</a></li>
|
||
|
||
<li>Familial endocrine adenomatosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/multiple-endocrine-neoplasia/">Multiple endocrine neoplasia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-erythrocytosis/">Familial erythrocytosis</a></li>
|
||
|
||
<li>Familial erythromelalgia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/erythromelalgia/">Erythromelalgia</a></li>
|
||
|
||
|
||
<li>Familial erythrophagocytic lymphohistiocytosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hemophagocytic-lymphohistiocytosis/">Familial hemophagocytic lymphohistiocytosis</a></li>
|
||
|
||
|
||
<li>Familial 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/familial-exudative-vitreoretinopathy/">Familial exudative vitreoretinopathy</a></li>
|
||
|
||
<li>Familial fat-induced hypertriglyceridemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-lipoprotein-lipase-deficiency/">Familial lipoprotein lipase deficiency</a></li>
|
||
|
||
|
||
<li>Familial fatal Epstein-Barr infection, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/x-linked-lymphoproliferative-disease/">X-linked lymphoproliferative disease</a></li>
|
||
|
||
|
||
<li>Familial fibrous dysplasia of jaw, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cherubism/">Cherubism</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-focal-epilepsy-with-variable-foci/">Familial focal epilepsy with variable foci</a></li>
|
||
|
||
<li>Familial glomerular nephritis with fibronectin deposits, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fibronectin-glomerulopathy/">Fibronectin glomerulopathy</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-glucocorticoid-deficiency/">Familial glucocorticoid deficiency</a></li>
|
||
|
||
<li>Familial gonadotrophin-independent sexual precocity, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-male-limited-precocious-puberty/">Familial male-limited precocious puberty</a></li>
|
||
|
||
|
||
<li>Familial granulomatosis, Blau type, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/blau-syndrome/">Blau syndrome</a></li>
|
||
|
||
|
||
<li>Familial gynecomastia due to increased aromatase activity, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/aromatase-excess-syndrome/">Aromatase excess syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-hdl-deficiency/">Familial HDL deficiency</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-hemiplegic-migraine/">Familial hemiplegic migraine</a></li>
|
||
|
||
<li>Familial hemochromatosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hemochromatosis/">Hereditary hemochromatosis</a></li>
|
||
|
||
|
||
<li>Familial hemophagocytic histiocytosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hemophagocytic-lymphohistiocytosis/">Familial hemophagocytic lymphohistiocytosis</a></li>
|
||
|
||
|
||
<li>Familial hemophagocytic lymphocytosis, <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/familial-hemophagocytic-lymphohistiocytosis/">Familial hemophagocytic lymphohistiocytosis</a></li>
|
||
|
||
<li>Familial hemophagocytic reticulosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hemophagocytic-lymphohistiocytosis/">Familial hemophagocytic lymphohistiocytosis</a></li>
|
||
|
||
|
||
<li>Familial Hibernian fever, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tumor-necrosis-factor-receptor-associated-periodic-syndrome/">Tumor necrosis factor receptor-associated periodic syndrome</a></li>
|
||
|
||
|
||
<li>Familial high density lipoprotein deficiency disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tangier-disease/">Tangier disease</a></li>
|
||
|
||
|
||
<li>Familial horizontal gaze palsy with progressive scoliosis, <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><a href="https://medlineplus.gov/genetics/condition/familial-hyperaldosteronism/">Familial hyperaldosteronism</a></li>
|
||
|
||
<li>Familial hypercalciuric hypocalcemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/autosomal-dominant-hypocalcemia/">Autosomal dominant hypocalcemia</a></li>
|
||
|
||
|
||
<li>Familial hypercholesterolaemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hypercholesterolemia/">Familial hypercholesterolemia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-hypercholesterolemia/">Familial hypercholesterolemia</a></li>
|
||
|
||
<li>Familial hyperchylomicronemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-lipoprotein-lipase-deficiency/">Familial lipoprotein lipase deficiency</a></li>
|
||
|
||
|
||
<li>Familial hyperekplexia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-hyperekplexia/">Hereditary hyperekplexia</a></li>
|
||
|
||
|
||
<li>Familial hyperkalemic hypertension, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pseudohypoaldosteronism-type-2/">Pseudohypoaldosteronism type 2</a></li>
|
||
|
||
|
||
<li>Familial hyperkalemic periodic paralysis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperkalemic-periodic-paralysis/">Hyperkalemic periodic paralysis</a></li>
|
||
|
||
|
||
<li>Familial hyperlysinemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperlysinemia/">Hyperlysinemia</a></li>
|
||
|
||
|
||
<li>Familial hyperpotassemia and hypertension, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pseudohypoaldosteronism-type-2/">Pseudohypoaldosteronism type 2</a></li>
|
||
|
||
|
||
<li>Familial hyperreninemic hypoaldosteronism, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/corticosterone-methyloxidase-deficiency/">Corticosterone methyloxidase deficiency</a></li>
|
||
|
||
|
||
<li>Familial hypertensive hyperkalemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pseudohypoaldosteronism-type-2/">Pseudohypoaldosteronism type 2</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-hypertrophic-cardiomyopathy/">Familial hypertrophic cardiomyopathy</a></li>
|
||
|
||
<li>Familial hypoalphalipoproteinemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hdl-deficiency/">Familial HDL deficiency</a></li>
|
||
|
||
|
||
<li>Familial hypoalphalipoproteinemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tangier-disease/">Tangier disease</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-hypobetalipoproteinemia/">Familial hypobetalipoproteinemia</a></li>
|
||
|
||
<li>Familial hypocalcemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/autosomal-dominant-hypocalcemia/">Autosomal dominant hypocalcemia</a></li>
|
||
|
||
|
||
<li>Familial hypokalemia-hypomagnesemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/gitelman-syndrome/">Gitelman syndrome</a></li>
|
||
|
||
|
||
<li>Familial hypokalemic periodic paralysis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypokalemic-periodic-paralysis/">Hypokalemic periodic paralysis</a></li>
|
||
|
||
|
||
<li>Familial idiopathic basal ganglia calcification, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/primary-familial-brain-calcification/">Primary familial brain calcification</a></li>
|
||
|
||
|
||
<li>Familial idiopathic cardiomyopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-dilated-cardiomyopathy/">Familial dilated cardiomyopathy</a></li>
|
||
|
||
|
||
<li>Familial idiopathic hyperphosphatasemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/juvenile-paget-disease/">Juvenile Paget disease</a></li>
|
||
|
||
|
||
<li>Familial idiopathic scoliosis associated with congenital encephalopathy, <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>Familial infantile encephalopathy with intracranial calcification and chronic cerebrospinal fluid lymphocytosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/aicardi-goutieres-syndrome/">Aicardi-Goutières syndrome</a></li>
|
||
|
||
|
||
<li>Familial infantile scoliosis associated with bilateral paralysis of conjugate gaze, <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>Familial infiltrative fibromatosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/desmoid-tumor/">Desmoid tumor</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-isolated-hyperparathyroidism/">Familial isolated hyperparathyroidism</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-isolated-pituitary-adenoma/">Familial isolated pituitary adenoma</a></li>
|
||
|
||
<li>Familial isolated vitamin E deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ataxia-with-vitamin-e-deficiency/">Ataxia with vitamin E deficiency</a></li>
|
||
|
||
|
||
<li>Familial juvenile gouty nephropathy, <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>Familial juvenile hyperuricemic nephropathy 1, <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>Familial juvenile hyperuricemic nephropathy 2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ren-related-kidney-disease/">REN-related kidney disease</a></li>
|
||
|
||
|
||
<li>Familial juvenile systemic granulomatosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/blau-syndrome/">Blau syndrome</a></li>
|
||
|
||
|
||
<li>Familial LCAT deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/complete-lcat-deficiency/">Complete LCAT deficiency</a></li>
|
||
|
||
|
||
<li>Familial lecithin-cholesterol acyltransferase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/complete-lcat-deficiency/">Complete LCAT deficiency</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-lipoprotein-lipase-deficiency/">Familial lipoprotein lipase deficiency</a></li>
|
||
|
||
<li>Familial lobular glomerulopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fibronectin-glomerulopathy/">Fibronectin glomerulopathy</a></li>
|
||
|
||
|
||
<li>Familial LPL deficiency, <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/familial-male-limited-precocious-puberty/">Familial male-limited precocious puberty</a></li>
|
||
|
||
<li>Familial manganese-induced neurotoxicity, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypermanganesemia-with-dystonia/">Hypermanganesemia with dystonia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-mediterranean-fever/">Familial Mediterranean fever</a></li>
|
||
|
||
<li>Familial multilocular cystic disease of the jaws, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cherubism/">Cherubism</a></li>
|
||
|
||
|
||
<li>Familial multiple polyposis syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-adenomatous-polyposis/">Familial adenomatous polyposis</a></li>
|
||
|
||
|
||
<li>Familial multiple trichoepitheliomata, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/multiple-familial-trichoepithelioma/">Multiple familial trichoepithelioma</a></li>
|
||
|
||
|
||
<li>Familial myoclonus with renal failure, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/action-myoclonus-renal-failure-syndrome/">Action myoclonus–renal failure syndrome</a></li>
|
||
|
||
|
||
<li>Familial nephrotic syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/congenital-nephrotic-syndrome/">Congenital nephrotic syndrome</a></li>
|
||
|
||
|
||
<li>Familial nodular heterotopia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/periventricular-heterotopia/">Periventricular heterotopia</a></li>
|
||
|
||
|
||
<li>Familial nonhemolytic jaundice, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/gilbert-syndrome/">Gilbert syndrome</a></li>
|
||
|
||
|
||
<li>Familial nonhemolytic unconjugated hyperbilirubinemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/crigler-najjar-syndrome/">Crigler-Najjar syndrome</a></li>
|
||
|
||
|
||
<li>Familial nonpolyposis colon cancer, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lynch-syndrome/">Lynch syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-osteochondritis-dissecans/">Familial osteochondritis dissecans</a></li>
|
||
|
||
<li>Familial osteodysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hajdu-cheney-syndrome/">Hajdu-Cheney syndrome</a></li>
|
||
|
||
|
||
<li>Familial osteoectasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/juvenile-paget-disease/">Juvenile Paget disease</a></li>
|
||
|
||
|
||
<li>Familial palmar fibromatosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dupuytren-contracture/">Dupuytren contracture</a></li>
|
||
|
||
|
||
<li>Familial pancreatitis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-pancreatitis/">Hereditary pancreatitis</a></li>
|
||
|
||
|
||
<li>Familial paraganglioma syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-paraganglioma-pheochromocytoma/">Hereditary paraganglioma-pheochromocytoma</a></li>
|
||
|
||
|
||
<li>Familial paraganglioma-pheochromocytoma syndromes, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-paraganglioma-pheochromocytoma/">Hereditary paraganglioma-pheochromocytoma</a></li>
|
||
|
||
|
||
<li>Familial paroxysmal choreoathetosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-paroxysmal-nonkinesigenic-dyskinesia/">Familial paroxysmal nonkinesigenic dyskinesia</a></li>
|
||
|
||
|
||
<li>Familial paroxysmal dystonia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-paroxysmal-kinesigenic-dyskinesia/">Familial paroxysmal kinesigenic dyskinesia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-paroxysmal-kinesigenic-dyskinesia/">Familial paroxysmal kinesigenic dyskinesia</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-paroxysmal-nonkinesigenic-dyskinesia/">Familial paroxysmal nonkinesigenic dyskinesia</a></li>
|
||
|
||
<li>Familial paroxysmal polyserositis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-mediterranean-fever/">Familial Mediterranean fever</a></li>
|
||
|
||
|
||
<li>Familial partial epilepsy with variable foci, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-focal-epilepsy-with-variable-foci/">Familial focal epilepsy with variable foci</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-partial-lipodystrophy/">Familial partial lipodystrophy</a></li>
|
||
|
||
<li>Familial persistent pulmonary hypertension of the newborn, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alveolar-capillary-dysplasia-with-misalignment-of-pulmonary-veins/">Alveolar capillary dysplasia with misalignment of pulmonary veins</a></li>
|
||
|
||
|
||
<li>Familial Pick's disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/frontotemporal-dementia-with-parkinsonism-17/">Frontotemporal dementia with parkinsonism-17</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-pityriasis-rubra-pilaris/">Familial pityriasis rubra pilaris</a></li>
|
||
|
||
<li>Familial polycythemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-erythrocytosis/">Familial erythrocytosis</a></li>
|
||
|
||
|
||
<li>Familial polymorphic ventricular tachycardia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/catecholaminergic-polymorphic-ventricular-tachycardia/">Catecholaminergic polymorphic ventricular tachycardia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-porencephaly/">Familial porencephaly</a></li>
|
||
|
||
<li>Familial posterior fossa brain tumor of infancy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/rhabdoid-tumor-predisposition-syndrome/">Rhabdoid tumor predisposition syndrome</a></li>
|
||
|
||
|
||
<li>Familial posterior fossa brain tumor syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/rhabdoid-tumor-predisposition-syndrome/">Rhabdoid tumor predisposition syndrome</a></li>
|
||
|
||
|
||
<li>Familial 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>Familial primary aldosteronism, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hyperaldosteronism/">Familial hyperaldosteronism</a></li>
|
||
|
||
|
||
<li>Familial primary hyperparathyroidism with multiple ossifying jaw fibromas, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hyperparathyroidism-jaw-tumor-syndrome/">Hyperparathyroidism-jaw tumor syndrome</a></li>
|
||
|
||
|
||
<li>Familial primary hypomagnesemia with hypocalcuria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hypomagnesemia-with-secondary-hypocalcemia/">Hypomagnesemia with secondary hypocalcemia</a></li>
|
||
|
||
|
||
<li>Familial primary pulmonary hypertension, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pulmonary-arterial-hypertension/">Pulmonary arterial hypertension</a></li>
|
||
|
||
|
||
<li>Familial progressive scleroderma, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/systemic-scleroderma/">Systemic scleroderma</a></li>
|
||
|
||
|
||
<li>Familial protracted enteropathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/microvillus-inclusion-disease/">Microvillus inclusion disease</a></li>
|
||
|
||
|
||
<li>Familial PRP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-pityriasis-rubra-pilaris/">Familial pityriasis rubra pilaris</a></li>
|
||
|
||
|
||
<li>Familial pterygium syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/multiple-pterygium-syndrome/">Multiple pterygium syndrome</a></li>
|
||
|
||
|
||
<li>Familial pyrimidemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/dihydropyrimidine-dehydrogenase-deficiency/">Dihydropyrimidine dehydrogenase deficiency</a></li>
|
||
|
||
|
||
<li>Familial rectal pain, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/paroxysmal-extreme-pain-disorder/">Paroxysmal extreme pain disorder</a></li>
|
||
|
||
|
||
<li>Familial recurrent hydatidiform mole, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/recurrent-hydatidiform-mole/">Recurrent hydatidiform mole</a></li>
|
||
|
||
|
||
<li>Familial renal hypouricaemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/renal-hypouricemia/">Renal hypouricemia</a></li>
|
||
|
||
|
||
<li>Familial renal hypouricemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/renal-hypouricemia/">Renal hypouricemia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-restrictive-cardiomyopathy/">Familial restrictive cardiomyopathy</a></li>
|
||
|
||
<li>Familial reticuloendotheliosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/omenn-syndrome/">Omenn syndrome</a></li>
|
||
|
||
|
||
<li>Familial retinal arterial macroaneurysm, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/retinal-arterial-macroaneurysm-with-supravalvular-pulmonic-stenosis/">Retinal arterial macroaneurysm with supravalvular pulmonic stenosis</a></li>
|
||
|
||
|
||
<li>Familial rhabdoid tumor, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/rhabdoid-tumor-predisposition-syndrome/">Rhabdoid tumor predisposition syndrome</a></li>
|
||
|
||
|
||
<li>Familial TAAD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-thoracic-aortic-aneurysm-and-dissection/">Familial thoracic aortic aneurysm and dissection</a></li>
|
||
|
||
|
||
<li>Familial thoracic aortic aneurysm, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-thoracic-aortic-aneurysm-and-dissection/">Familial thoracic aortic aneurysm and dissection</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/familial-thoracic-aortic-aneurysm-and-dissection/">Familial thoracic aortic aneurysm and dissection</a></li>
|
||
|
||
<li>Familial thrombotic thrombocytopenia purpura, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/thrombotic-thrombocytopenic-purpura/">Thrombotic thrombocytopenic purpura</a></li>
|
||
|
||
|
||
<li>Familial tremor, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/essential-tremor/">Essential tremor</a></li>
|
||
|
||
|
||
<li>Familial Turner syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/noonan-syndrome/">Noonan syndrome</a></li>
|
||
|
||
|
||
<li>Familial vascular leukoencephalopathy, <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>Familial veno-occlusive 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>Familial visceral myopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/intestinal-pseudo-obstruction/">Intestinal pseudo-obstruction</a></li>
|
||
|
||
|
||
<li>Familial visceral neuropathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/intestinal-pseudo-obstruction/">Intestinal pseudo-obstruction</a></li>
|
||
|
||
|
||
<li>Familial visceral xanthomatosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lysosomal-acid-lipase-deficiency/">Lysosomal acid lipase deficiency</a></li>
|
||
|
||
|
||
<li>Familial white folded mucosal dysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/white-sponge-nevus/">White sponge nevus</a></li>
|
||
|
||
|
||
<li>Familial xanthomatosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/lysosomal-acid-lipase-deficiency/">Lysosomal acid lipase deficiency</a></li>
|
||
|
||
|
||
<li>Familial young-adult-onset arteriosclerotic leukoencephalopathy with alopecia and lumbago without arterial hypertension, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cerebral-autosomal-recessive-arteriopathy-with-subcortical-infarcts-and-leukoencephalopathy/">Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fanconi-anemia/">Fanconi anemia</a></li>
|
||
|
||
<li>Fanconi hypoplastic anemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fanconi-anemia/">Fanconi anemia</a></li>
|
||
|
||
|
||
<li>Fanconi pancytopenia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fanconi-anemia/">Fanconi anemia</a></li>
|
||
|
||
|
||
<li>Fanconi panmyelopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fanconi-anemia/">Fanconi anemia</a></li>
|
||
|
||
|
||
<li>FAP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-adenomatous-polyposis/">Familial adenomatous polyposis</a></li>
|
||
|
||
|
||
<li>Far-sightedness, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/farsightedness/">Farsightedness</a></li>
|
||
|
||
|
||
<li>Farber disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/farber-lipogranulomatosis/">Farber lipogranulomatosis</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/farber-lipogranulomatosis/">Farber lipogranulomatosis</a></li>
|
||
|
||
<li>Farber's disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/farber-lipogranulomatosis/">Farber lipogranulomatosis</a></li>
|
||
|
||
|
||
<li>Farber's lipogranulomatosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/farber-lipogranulomatosis/">Farber lipogranulomatosis</a></li>
|
||
|
||
|
||
<li>Farber-Uzman syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/farber-lipogranulomatosis/">Farber lipogranulomatosis</a></li>
|
||
|
||
|
||
<li>Farsighted, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/farsightedness/">Farsightedness</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/farsightedness/">Farsightedness</a></li>
|
||
|
||
<li>Fatal infantile lactic acidosis with methylmalonic aciduria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/suclg1-related-mitochondrial-dna-depletion-syndrome/">SUCLG1-related mitochondrial DNA depletion syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fatty-acid-hydroxylase-associated-neurodegeneration/">Fatty acid hydroxylase-associated neurodegeneration</a></li>
|
||
|
||
<li>Fatty aldehyde dehydrogenase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/sjogren-larsson-syndrome/">Sjögren-Larsson syndrome</a></li>
|
||
|
||
|
||
<li>Fatty liver, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/non-alcoholic-fatty-liver-disease/">Non-alcoholic fatty liver disease</a></li>
|
||
|
||
|
||
<li>FAV, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/craniofacial-microsomia/">Craniofacial microsomia</a></li>
|
||
|
||
|
||
<li>Fazio-Londe disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/riboflavin-transporter-deficiency-neuronopathy/">Riboflavin transporter deficiency neuronopathy</a></li>
|
||
|
||
|
||
<li>Fazio-Londe syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/riboflavin-transporter-deficiency-neuronopathy/">Riboflavin transporter deficiency neuronopathy</a></li>
|
||
|
||
|
||
<li>FBCG1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fibrochondrogenesis/">Fibrochondrogenesis</a></li>
|
||
|
||
|
||
<li>FBCG2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fibrochondrogenesis/">Fibrochondrogenesis</a></li>
|
||
|
||
|
||
<li>FBS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/freeman-sheldon-syndrome/">Freeman-Sheldon syndrome</a></li>
|
||
|
||
|
||
<li>FBXL4 deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fbxl4-related-encephalomyopathic-mitochondrial-dna-depletion-syndrome/">FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome</a></li>
|
||
|
||
|
||
<li>FBXL4-related early onset mitochondrial encephalopathy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fbxl4-related-encephalomyopathic-mitochondrial-dna-depletion-syndrome/">FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fbxl4-related-encephalomyopathic-mitochondrial-dna-depletion-syndrome/">FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome</a></li>
|
||
|
||
<li>FCAS2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-cold-autoinflammatory-syndrome-type-2/">Familial cold autoinflammatory syndrome type 2</a></li>
|
||
|
||
|
||
<li>FCAS3, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/plcg2-associated-antibody-deficiency-and-immune-dysregulation/">PLCG2-associated antibody deficiency and immune dysregulation</a></li>
|
||
|
||
|
||
<li>FCMD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fukuyama-congenital-muscular-dystrophy/">Fukuyama congenital muscular dystrophy</a></li>
|
||
|
||
|
||
<li>FCS syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/costello-syndrome/">Costello syndrome</a></li>
|
||
|
||
|
||
<li>FD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-dysautonomia/">Familial dysautonomia</a></li>
|
||
|
||
|
||
<li>FDC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-dilated-cardiomyopathy/">Familial dilated cardiomyopathy</a></li>
|
||
|
||
|
||
<li>FDFM, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/adcy5-related-dyskinesia/">ADCY5-related dyskinesia</a></li>
|
||
|
||
|
||
<li>FDGC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-diffuse-gastric-cancer/">Hereditary diffuse gastric cancer</a></li>
|
||
|
||
|
||
<li>FED, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fish-eye-disease/">Fish-eye disease</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/feingold-syndrome/">Feingold syndrome</a></li>
|
||
|
||
<li>FEL, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hemophagocytic-lymphohistiocytosis/">Familial hemophagocytic lymphohistiocytosis</a></li>
|
||
|
||
|
||
<li>Fellman syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/gracile-syndrome/">GRACILE syndrome</a></li>
|
||
|
||
|
||
<li>Female pattern baldness, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/androgenetic-alopecia/">Androgenetic alopecia</a></li>
|
||
|
||
|
||
<li>Female pseudo-Turner syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/noonan-syndrome/">Noonan syndrome</a></li>
|
||
|
||
|
||
<li>Female-pattern hair loss, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/androgenetic-alopecia/">Androgenetic alopecia</a></li>
|
||
|
||
|
||
<li>Fenestrae parietals symmetricae, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/enlarged-parietal-foramina/">Enlarged parietal foramina</a></li>
|
||
|
||
|
||
<li>FENIB, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-encephalopathy-with-neuroserpin-inclusion-bodies/">Familial encephalopathy with neuroserpin inclusion bodies</a></li>
|
||
|
||
|
||
<li>Ferritin-related neurodegeneration, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/neuroferritinopathy/">Neuroferritinopathy</a></li>
|
||
|
||
|
||
<li>FESD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum/">Epilepsy-aphasia spectrum</a></li>
|
||
|
||
|
||
<li>Fetal face syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/robinow-syndrome/">Robinow syndrome</a></li>
|
||
|
||
|
||
<li>Fetal iritis syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/norrie-disease/">Norrie disease</a></li>
|
||
|
||
|
||
<li>Fetal myocardium, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/left-ventricular-noncompaction/">Left ventricular noncompaction</a></li>
|
||
|
||
|
||
<li>FEVR, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-exudative-vitreoretinopathy/">Familial exudative vitreoretinopathy</a></li>
|
||
|
||
|
||
<li>FFEVF, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-focal-epilepsy-with-variable-foci/">Familial focal epilepsy with variable foci</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fg-syndrome/">FG syndrome</a></li>
|
||
|
||
<li>FGDY, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/aarskog-scott-syndrome/">Aarskog-Scott syndrome</a></li>
|
||
|
||
|
||
<li>FGFR1-related osteoglophonic dysplasia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/osteoglophonic-dysplasia/">Osteoglophonic dysplasia</a></li>
|
||
|
||
|
||
<li>FGFR3-associated coronal synostosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/muenke-syndrome/">Muenke syndrome</a></li>
|
||
|
||
|
||
<li>FGS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fg-syndrome/">FG syndrome</a></li>
|
||
|
||
|
||
<li>FGS1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fg-syndrome/">FG syndrome</a></li>
|
||
|
||
|
||
<li>FH, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hypercholesterolemia/">Familial hypercholesterolemia</a></li>
|
||
|
||
|
||
<li>FH, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hyperaldosteronism/">Familial hyperaldosteronism</a></li>
|
||
|
||
|
||
<li>FHA, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hdl-deficiency/">Familial HDL deficiency</a></li>
|
||
|
||
|
||
<li>FHBL, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hypobetalipoproteinemia/">Familial hypobetalipoproteinemia</a></li>
|
||
|
||
|
||
<li>FHHt, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pseudohypoaldosteronism-type-2/">Pseudohypoaldosteronism type 2</a></li>
|
||
|
||
|
||
<li>FHL, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hemophagocytic-lymphohistiocytosis/">Familial hemophagocytic lymphohistiocytosis</a></li>
|
||
|
||
|
||
<li>FHLH, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-hemophagocytic-lymphohistiocytosis/">Familial hemophagocytic lymphohistiocytosis</a></li>
|
||
|
||
|
||
<li>FHS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/floating-harbor-syndrome/">Floating-Harbor syndrome</a></li>
|
||
|
||
|
||
<li>FIBGC, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/primary-familial-brain-calcification/">Primary familial brain calcification</a></li>
|
||
|
||
|
||
<li>Fibrin stabilizing factor deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/factor-xiii-deficiency/">Factor XIII deficiency</a></li>
|
||
|
||
|
||
<li>Fibrinoid degeneration of astrocytes, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/alexander-disease/">Alexander disease</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fibrochondrogenesis/">Fibrochondrogenesis</a></li>
|
||
|
||
<li>Fibrochondrogenesis-1, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fibrochondrogenesis/">Fibrochondrogenesis</a></li>
|
||
|
||
|
||
<li>Fibrochondrogenesis-2, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fibrochondrogenesis/">Fibrochondrogenesis</a></li>
|
||
|
||
|
||
<li>Fibrocystic disease of pancreas, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cystic-fibrosis/">Cystic fibrosis</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fibrodysplasia-ossificans-progressiva/">Fibrodysplasia ossificans progressiva</a></li>
|
||
|
||
<li>Fibrofolliculomas with trichodiscomas and acrochordons, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/birt-hogg-dube-syndrome/">Birt-Hogg-Dubé syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fibromyalgia/">Fibromyalgia</a></li>
|
||
|
||
<li>Fibromyalgia syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fibromyalgia/">Fibromyalgia</a></li>
|
||
|
||
|
||
<li>Fibromyalgia-fibromyositis syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fibromyalgia/">Fibromyalgia</a></li>
|
||
|
||
|
||
<li>Fibromyositis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fibromyalgia/">Fibromyalgia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fibronectin-glomerulopathy/">Fibronectin glomerulopathy</a></li>
|
||
|
||
<li>Fibrositis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fibromyalgia/">Fibromyalgia</a></li>
|
||
|
||
|
||
<li>Fibrous dysplasia with pigmentary skin changes and precocious puberty, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/mccune-albright-syndrome/">McCune-Albright syndrome</a></li>
|
||
|
||
|
||
<li>FIC1 deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/progressive-familial-intrahepatic-cholestasis/">Progressive familial intrahepatic cholestasis</a></li>
|
||
|
||
|
||
<li>Fifth digit syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/coffin-siris-syndrome/">Coffin-Siris syndrome</a></li>
|
||
|
||
|
||
<li>FIGLU-uria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glutamate-formiminotransferase-deficiency/">Glutamate formiminotransferase deficiency</a></li>
|
||
|
||
|
||
<li>FIHP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-isolated-hyperparathyroidism/">Familial isolated hyperparathyroidism</a></li>
|
||
|
||
|
||
<li>Filamin-A-associated myxomatous mitral valve disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/x-linked-cardiac-valvular-dysplasia/">X-linked cardiac valvular dysplasia</a></li>
|
||
|
||
|
||
<li>Filamin-A-related myxomatous mitral valve dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/x-linked-cardiac-valvular-dysplasia/">X-linked cardiac valvular dysplasia</a></li>
|
||
|
||
|
||
<li>Finlay-Marks syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/scalp-ear-nipple-syndrome/">Scalp-ear-nipple syndrome</a></li>
|
||
|
||
|
||
<li>Finnish lactic acidosis with hepatic hemosiderosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/gracile-syndrome/">GRACILE syndrome</a></li>
|
||
|
||
|
||
<li>Finnish lethal neonatal metabolic syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/gracile-syndrome/">GRACILE syndrome</a></li>
|
||
|
||
|
||
<li>Finnish variant late infantile neuronal ceroid lipofuscinosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cln5-disease/">CLN5 disease</a></li>
|
||
|
||
|
||
<li>Finnish vLINCL, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cln5-disease/">CLN5 disease</a></li>
|
||
|
||
|
||
<li>FIPA, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-isolated-pituitary-adenoma/">Familial isolated pituitary adenoma</a></li>
|
||
|
||
|
||
<li>First and second branchial arch syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/craniofacial-microsomia/">Craniofacial microsomia</a></li>
|
||
|
||
|
||
<li>First and second pharyngeal arch syndromes, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/craniofacial-microsomia/">Craniofacial microsomia</a></li>
|
||
|
||
|
||
<li>Fish malodor syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trimethylaminuria/">Trimethylaminuria</a></li>
|
||
|
||
|
||
<li>Fish odor syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/trimethylaminuria/">Trimethylaminuria</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fish-eye-disease/">Fish-eye disease</a></li>
|
||
|
||
<li>Fisher syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/guillain-barre-syndrome/">Guillain-Barré syndrome</a></li>
|
||
|
||
|
||
<li>Fishman syndrome (formerly), <i>see</i> <a href="https://medlineplus.gov/genetics/condition/encephalocraniocutaneous-lipomatosis/">Encephalocraniocutaneous lipomatosis</a></li>
|
||
|
||
|
||
<li>FIVE, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ataxia-with-vitamin-e-deficiency/">Ataxia with vitamin E deficiency</a></li>
|
||
|
||
|
||
<li>FJHN, <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>FKTN-related congenital muscular dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fukuyama-congenital-muscular-dystrophy/">Fukuyama congenital muscular dystrophy</a></li>
|
||
|
||
|
||
<li>FLD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/complete-lcat-deficiency/">Complete LCAT deficiency</a></li>
|
||
|
||
|
||
<li>Fletcher factor deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/prekallikrein-deficiency/">Prekallikrein deficiency</a></li>
|
||
|
||
|
||
<li>Fletcher trait, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/prekallikrein-deficiency/">Prekallikrein deficiency</a></li>
|
||
|
||
|
||
<li>FLHS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/floating-harbor-syndrome/">Floating-Harbor syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/floating-harbor-syndrome/">Floating-Harbor syndrome</a></li>
|
||
|
||
<li>Flowing hyperostosis, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/melorheostosis/">Melorheostosis</a></li>
|
||
|
||
|
||
<li>FMD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/frontometaphyseal-dysplasia/">Frontometaphyseal dysplasia</a></li>
|
||
|
||
|
||
<li>FMF, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-mediterranean-fever/">Familial Mediterranean fever</a></li>
|
||
|
||
|
||
<li>FMR1-related primary ovarian insufficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fragile-x-associated-primary-ovarian-insufficiency/">Fragile X-associated primary ovarian insufficiency</a></li>
|
||
|
||
|
||
<li>FMS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fibromyalgia/">Fibromyalgia</a></li>
|
||
|
||
|
||
<li>FND, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/frontonasal-dysplasia/">Frontonasal dysplasia</a></li>
|
||
|
||
|
||
<li>FNM, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/frontonasal-dysplasia/">Frontonasal dysplasia</a></li>
|
||
|
||
|
||
<li>FOAR syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/donnai-barrow-syndrome/">Donnai-Barrow syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/focal-dermal-hypoplasia/">Focal dermal hypoplasia</a></li>
|
||
|
||
<li>Focal epilepsies with speech and language disorders, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum/">Epilepsy-aphasia spectrum</a></li>
|
||
|
||
|
||
<li>Focal epilepsy with speech disorder and with or without mental retardation, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum/">Epilepsy-aphasia spectrum</a></li>
|
||
|
||
|
||
<li>Focal hand dystonia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/task-specific-focal-dystonia/">Task-specific focal dystonia</a></li>
|
||
|
||
|
||
<li>Focal task-specific dystonia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/task-specific-focal-dystonia/">Task-specific focal dystonia</a></li>
|
||
|
||
|
||
<li>FOCD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-osteochondritis-dissecans/">Familial osteochondritis dissecans</a></li>
|
||
|
||
|
||
<li>Folic acid transport defect, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-folate-malabsorption/">Hereditary folate malabsorption</a></li>
|
||
|
||
|
||
<li>Folling disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/phenylketonuria/">Phenylketonuria</a></li>
|
||
|
||
|
||
<li>Folling's disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/phenylketonuria/">Phenylketonuria</a></li>
|
||
|
||
|
||
<li>FOLR1 deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/cerebral-folate-transport-deficiency/">Cerebral folate transport deficiency</a></li>
|
||
|
||
|
||
<li>Fong disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/nail-patella-syndrome/">Nail-patella syndrome</a></li>
|
||
|
||
|
||
<li>FOP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fibrodysplasia-ossificans-progressiva/">Fibrodysplasia ossificans progressiva</a></li>
|
||
|
||
|
||
<li>Foramina parietalia permagna, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/enlarged-parietal-foramina/">Enlarged parietal foramina</a></li>
|
||
|
||
|
||
<li>Forbes disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glycogen-storage-disease-type-iii/">Glycogen storage disease type III</a></li>
|
||
|
||
|
||
<li>Formiminoglutamic aciduria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glutamate-formiminotransferase-deficiency/">Glutamate formiminotransferase deficiency</a></li>
|
||
|
||
|
||
<li>Formiminotransferase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/glutamate-formiminotransferase-deficiency/">Glutamate formiminotransferase deficiency</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/foxg1-syndrome/">FOXG1 syndrome</a></li>
|
||
|
||
<li>FOXG1-related disorder, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/foxg1-syndrome/">FOXG1 syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/foxp2-related-speech-and-language-disorder/">FOXP2-related speech and language disorder</a></li>
|
||
|
||
<li>FPF, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/tumor-necrosis-factor-receptor-associated-periodic-syndrome/">Tumor necrosis factor receptor-associated periodic syndrome</a></li>
|
||
|
||
|
||
<li>FPGL, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-paraganglioma-pheochromocytoma/">Hereditary paraganglioma-pheochromocytoma</a></li>
|
||
|
||
|
||
<li>FPGL/PHEO, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-paraganglioma-pheochromocytoma/">Hereditary paraganglioma-pheochromocytoma</a></li>
|
||
|
||
|
||
<li>FPL, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-partial-lipodystrophy/">Familial partial lipodystrophy</a></li>
|
||
|
||
|
||
<li>FPO, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/otopalatodigital-syndrome-type-1/">Otopalatodigital syndrome type 1</a></li>
|
||
|
||
|
||
<li>FPO, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/otopalatodigital-syndrome-type-2/">Otopalatodigital syndrome type 2</a></li>
|
||
|
||
|
||
<li>FPP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/enlarged-parietal-foramina/">Enlarged parietal foramina</a></li>
|
||
|
||
|
||
<li>FPPH, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/pulmonary-arterial-hypertension/">Pulmonary arterial hypertension</a></li>
|
||
|
||
|
||
<li>FPVT, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/catecholaminergic-polymorphic-ventricular-tachycardia/">Catecholaminergic polymorphic ventricular tachycardia</a></li>
|
||
|
||
|
||
<li>Fra(X) syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fragile-x-syndrome/">Fragile X syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fragile-x-syndrome/">Fragile X syndrome</a></li>
|
||
|
||
<li>Fragile X tremor/ataxia syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fragile-x-associated-tremor-ataxia-syndrome/">Fragile X-associated tremor/ataxia syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fragile-x-associated-primary-ovarian-insufficiency/">Fragile X-associated primary ovarian insufficiency</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fragile-x-associated-tremor-ataxia-syndrome/">Fragile X-associated tremor/ataxia syndrome</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fragile-xe-syndrome/">Fragile XE syndrome</a></li>
|
||
|
||
<li>Fragilitas ossium, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/osteogenesis-imperfecta/">Osteogenesis imperfecta</a></li>
|
||
|
||
|
||
<li>FRAM, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/retinal-arterial-macroaneurysm-with-supravalvular-pulmonic-stenosis/">Retinal arterial macroaneurysm with supravalvular pulmonic stenosis</a></li>
|
||
|
||
|
||
<li>Franceschetti-Jadassohn syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/naegeli-franceschetti-jadassohn-syndrome-dermatopathia-pigmentosa-reticularis/">Naegeli-Franceschetti-Jadassohn syndrome/dermatopathia pigmentosa reticularis</a></li>
|
||
|
||
|
||
<li>Franceschetti-Zwahlen-Klein syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/treacher-collins-syndrome/">Treacher Collins syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fraser-syndrome/">Fraser syndrome</a></li>
|
||
|
||
<li>Fraser's syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fraser-syndrome/">Fraser syndrome</a></li>
|
||
|
||
|
||
<li>Fraser-Francois syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fraser-syndrome/">Fraser syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/frasier-syndrome/">Frasier syndrome</a></li>
|
||
|
||
<li>FRAXA syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fragile-x-syndrome/">Fragile X syndrome</a></li>
|
||
|
||
|
||
<li>FRAXE intellectual deficit, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fragile-xe-syndrome/">Fragile XE syndrome</a></li>
|
||
|
||
|
||
<li>FRAXE intellectual disability, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fragile-xe-syndrome/">Fragile XE syndrome</a></li>
|
||
|
||
|
||
<li>FRAXE syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fragile-xe-syndrome/">Fragile XE syndrome</a></li>
|
||
|
||
|
||
<li>FRDA, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/friedreich-ataxia/">Friedreich ataxia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/free-sialic-acid-storage-disorder/">Free sialic acid storage disorder</a></li>
|
||
|
||
<li>Freeman-Burian syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/freeman-sheldon-syndrome/">Freeman-Sheldon syndrome</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/freeman-sheldon-syndrome/">Freeman-Sheldon syndrome</a></li>
|
||
|
||
<li>French type sialuria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/sialuria/">Sialuria</a></li>
|
||
|
||
|
||
<li>FRHM, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/recurrent-hydatidiform-mole/">Recurrent hydatidiform mole</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/friedreich-ataxia/">Friedreich ataxia</a></li>
|
||
|
||
<li>Friedreich ataxia phenotype with selective vitamin E deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ataxia-with-vitamin-e-deficiency/">Ataxia with vitamin E deficiency</a></li>
|
||
|
||
|
||
<li>Friedreich spinocerebellar ataxia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/friedreich-ataxia/">Friedreich ataxia</a></li>
|
||
|
||
|
||
<li>Friedreich-like ataxia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/ataxia-with-vitamin-e-deficiency/">Ataxia with vitamin E deficiency</a></li>
|
||
|
||
|
||
<li>Friedrich's ataxia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/friedreich-ataxia/">Friedreich ataxia</a></li>
|
||
|
||
|
||
<li>FRMD7-related infantile nystagmus, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/x-linked-infantile-nystagmus/">X-linked infantile nystagmus</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/frontometaphyseal-dysplasia/">Frontometaphyseal dysplasia</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/frontonasal-dysplasia/">Frontonasal dysplasia</a></li>
|
||
|
||
<li>Frontonasal dysplasia sequence, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/frontonasal-dysplasia/">Frontonasal dysplasia</a></li>
|
||
|
||
|
||
<li>Frontonasal malformation, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/frontonasal-dysplasia/">Frontonasal dysplasia</a></li>
|
||
|
||
|
||
<li>Frontorhiny, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/frontonasal-dysplasia/">Frontonasal dysplasia</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/frontotemporal-dementia-with-parkinsonism-17/">Frontotemporal dementia with parkinsonism-17</a></li>
|
||
|
||
<li>Frontotemporal lobar degeneration, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/grn-related-frontotemporal-lobar-degeneration/">GRN-related frontotemporal lobar degeneration</a></li>
|
||
|
||
|
||
<li>Fructose aldolase B deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-fructose-intolerance/">Hereditary fructose intolerance</a></li>
|
||
|
||
|
||
<li>Fructose intolerance, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-fructose-intolerance/">Hereditary fructose intolerance</a></li>
|
||
|
||
|
||
<li>Fructose-1,6-biphosphate aldolase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-fructose-intolerance/">Hereditary fructose intolerance</a></li>
|
||
|
||
|
||
<li>Fructose-1-phosphate aldolase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-fructose-intolerance/">Hereditary fructose intolerance</a></li>
|
||
|
||
|
||
<li>Fructosemia, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/hereditary-fructose-intolerance/">Hereditary fructose intolerance</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fryns-syndrome/">Fryns syndrome</a></li>
|
||
|
||
<li>Fryns-Aftimos syndrome, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/baraitser-winter-syndrome/">Baraitser-Winter syndrome</a></li>
|
||
|
||
|
||
<li>FS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/frasier-syndrome/">Frasier syndrome</a></li>
|
||
|
||
|
||
<li>FSASD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/free-sialic-acid-storage-disorder/">Free sialic acid storage disorder</a></li>
|
||
|
||
|
||
<li>FSH muscular dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/facioscapulohumeral-muscular-dystrophy/">Facioscapulohumeral muscular dystrophy</a></li>
|
||
|
||
|
||
<li>FSHD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/facioscapulohumeral-muscular-dystrophy/">Facioscapulohumeral muscular dystrophy</a></li>
|
||
|
||
|
||
<li>FSS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/freeman-sheldon-syndrome/">Freeman-Sheldon syndrome</a></li>
|
||
|
||
|
||
<li>FTAAD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/familial-thoracic-aortic-aneurysm-and-dissection/">Familial thoracic aortic aneurysm and dissection</a></li>
|
||
|
||
|
||
<li>FTD-3, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/chmp2b-related-frontotemporal-dementia/">CHMP2B-related frontotemporal dementia</a></li>
|
||
|
||
|
||
<li>FTD-CHMP2B, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/chmp2b-related-frontotemporal-dementia/">CHMP2B-related frontotemporal dementia</a></li>
|
||
|
||
|
||
<li>FTD-GRN, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/grn-related-frontotemporal-lobar-degeneration/">GRN-related frontotemporal lobar degeneration</a></li>
|
||
|
||
|
||
<li>FTD-PGRN, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/grn-related-frontotemporal-lobar-degeneration/">GRN-related frontotemporal lobar degeneration</a></li>
|
||
|
||
|
||
<li>FTD3, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/chmp2b-related-frontotemporal-dementia/">CHMP2B-related frontotemporal dementia</a></li>
|
||
|
||
|
||
<li>FTDP-17, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/frontotemporal-dementia-with-parkinsonism-17/">Frontotemporal dementia with parkinsonism-17</a></li>
|
||
|
||
|
||
<li>FTDP-17 GRN, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/grn-related-frontotemporal-lobar-degeneration/">GRN-related frontotemporal lobar degeneration</a></li>
|
||
|
||
|
||
<li>FTDU-17, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/grn-related-frontotemporal-lobar-degeneration/">GRN-related frontotemporal lobar degeneration</a></li>
|
||
|
||
|
||
<li>FTLD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/grn-related-frontotemporal-lobar-degeneration/">GRN-related frontotemporal lobar degeneration</a></li>
|
||
|
||
|
||
<li>FTLD with TDP-43 pathology, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/grn-related-frontotemporal-lobar-degeneration/">GRN-related frontotemporal lobar degeneration</a></li>
|
||
|
||
|
||
<li>FTLD-TDP, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/grn-related-frontotemporal-lobar-degeneration/">GRN-related frontotemporal lobar degeneration</a></li>
|
||
|
||
|
||
<li>FTSD, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/task-specific-focal-dystonia/">Task-specific focal dystonia</a></li>
|
||
|
||
|
||
<li>Fuchs atrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fuchs-endothelial-dystrophy/">Fuchs endothelial dystrophy</a></li>
|
||
|
||
|
||
<li>Fuchs corneal dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fuchs-endothelial-dystrophy/">Fuchs endothelial dystrophy</a></li>
|
||
|
||
|
||
<li>Fuchs dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fuchs-endothelial-dystrophy/">Fuchs endothelial dystrophy</a></li>
|
||
|
||
|
||
<li>Fuchs endothelial corneal dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fuchs-endothelial-dystrophy/">Fuchs endothelial dystrophy</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fuchs-endothelial-dystrophy/">Fuchs endothelial dystrophy</a></li>
|
||
|
||
<li>Fuchs' endothelial dystrophy, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fuchs-endothelial-dystrophy/">Fuchs endothelial dystrophy</a></li>
|
||
|
||
|
||
<li>Fucosidase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fucosidosis/">Fucosidosis</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fucosidosis/">Fucosidosis</a></li>
|
||
|
||
<li>Fukuhara disease, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/myoclonic-epilepsy-with-ragged-red-fibers/">Myoclonic epilepsy with ragged-red fibers</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fukuyama-congenital-muscular-dystrophy/">Fukuyama congenital muscular dystrophy</a></li>
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fumarase-deficiency/">Fumarase deficiency</a></li>
|
||
|
||
<li>Fumarate hydratase deficiency, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fumarase-deficiency/">Fumarase deficiency</a></li>
|
||
|
||
|
||
<li>Fumaric aciduria, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fumarase-deficiency/">Fumarase deficiency</a></li>
|
||
|
||
|
||
<li><a href="https://medlineplus.gov/genetics/condition/fundus-albipunctatus/">Fundus albipunctatus</a></li>
|
||
|
||
<li>Fusion of cervical vertebrae, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/klippel-feil-syndrome/">Klippel-Feil syndrome</a></li>
|
||
|
||
|
||
<li>FXPOI, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fragile-x-associated-primary-ovarian-insufficiency/">Fragile X-associated primary ovarian insufficiency</a></li>
|
||
|
||
|
||
<li>FXS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fragile-x-syndrome/">Fragile X syndrome</a></li>
|
||
|
||
|
||
<li>FXTAS, <i>see</i> <a href="https://medlineplus.gov/genetics/condition/fragile-x-associated-tremor-ataxia-syndrome/">Fragile X-associated tremor/ataxia syndrome</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-f/" 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>
|