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<meta name="keywords" content="C0238339, autosomal dominant hereditary pancreatitis, cftr, ctrc, disease or syndrome, familial chronic pancreatitis, familial pancreatitis, hereditary chronic pancreatitis, hereditary pancreatitis, hp, hpc, pancreatitis, calcific, pancreatitis, calcific, included, pancreatitis, chronic, pancreatitis, chronic pancreatitis, chronic, susceptibility to, included, pancreatitis, chronic, protection against, pancreatitis, chronic, protection against, included, pancreatitis, chronic, susceptibility to, pancreatitis, hereditary, pctt, prss1, prss2, spink1, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="PRSS1-related hereditary pancreatitis (HP) is characterized by episodes of acute pancreatitis (AP) and recurrent acute pancreatitis (RAP: >1 episode of AP), with frequent progression to chronic pancreatitis (CP). Manifestations of acute pancreatitis can range from vague abdominal pain lasting one to three days to severe abdominal pain lasting days to weeks and requiring hospitalization." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=116056
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ConceptID=C0238339
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Hereditary pancreatitis<span class="h1sub">(PCTT)</span></div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>116056</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information."><span class="highlight" style="background-color:">C0238339</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Hereditary chronic pancreatitis; PCTT</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Hereditary pancreatitis (68072000); Familial chronic pancreatitis (235956004); Hereditary chronic pancreatitis (235956004)</td></tr>
|
||
<tr><td>Modes of inheritance:</td>
|
||
<td>
|
||
<div class="divPopper rprt" id="moi_141047"><div><strong>Autosomal dominant inheritance</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>141047</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0443147</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Intellectual Product</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Source: Orphanet</div>
|
||
<div class="spaceAbove">A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.</div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#moi_141047" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal dominant inheritance</a><span> (Orphanet)</span></div></td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td><a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#target-gene-loc">Genes (locations):<img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a><div class="display-none" id="target-gene-loc">
|
||
Gene(s) directly associated with<br />
|
||
this condition or phenotype.</div></td>
|
||
<td><a target="_blank" title="CFTR - ID: 1080 - NCBI Gene" href="/gene/1080" class="medgenPMinfo">CFTR</a> (7q31.2); <a target="_blank" title="CTRC - ID: 11330 - NCBI Gene" href="/gene/11330" class="medgenPMinfo">CTRC</a> (1p36.21); <a target="_blank" title="PRSS1 - ID: 5644 - NCBI Gene" href="/gene/5644" class="medgenPMinfo">PRSS1</a> (7q34); <a target="_blank" title="PRSS2 - ID: 5645 - NCBI Gene" href="/gene/5645" class="medgenPMinfo">PRSS2</a> (7q34); <a target="_blank" title="SPINK1 - ID: 6690 - NCBI Gene" href="/gene/6690" class="medgenPMinfo">SPINK1</a> (5q32)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0008185" target="_blank">MONDO:0008185</a></td></tr>
|
||
<tr><td>OMIM<span class="superscript">®</span>:</td>
|
||
<td><a href="https://omim.org/entry/167800" target="_blank">167800</a></td></tr>
|
||
<tr><td>Orphanet:</td>
|
||
<td><a target="_blank" title="Orphanet: The portal for rare diseases and orphan drugs" href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=676">ORPHA676</a></td></tr></tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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<div class="portlet mgSection" id="ID_100">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">PRSS1-related hereditary pancreatitis (HP) is characterized by episodes of acute pancreatitis (AP) and recurrent acute pancreatitis (RAP: >1 episode of AP), with frequent progression to chronic pancreatitis (CP). Manifestations of acute pancreatitis can range from vague abdominal pain lasting one to three days to severe abdominal pain lasting days to weeks and requiring hospitalization. [from <a title="GeneReviews" href="https://www.ncbi.nlm.nih.gov/books/NBK1116" class="defSource" target="_blank">GeneReviews</a>]</div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_117">
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||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Additional_description">Additional description</h1><a sid="117" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><div class="mgSection"><strong>From MedlinePlus Genetics</strong><br />Hereditary pancreatitis is a genetic condition characterized by recurrent episodes of inflammation of the pancreas (pancreatitis). The pancreas produces enzymes that help digest food, and it also produces insulin, a hormone that controls levels of blood glucose, also called blood sugar. Episodes of pancreatitis can lead to permanent tissue damage and loss of pancreatic function.<br /><br />Signs and symptoms of this condition usually begin in late childhood with an episode of acute pancreatitis. A sudden (acute) attack can cause abdominal pain, fever, nausea, or vomiting. An episode typically lasts from one to three days, although some people may experience severe episodes that last longer. Hereditary pancreatitis progresses to recurrent acute pancreatitis with multiple episodes of acute pancreatitis that recur over a period of at least a year; the number of episodes a person experiences varies. Recurrent acute pancreatitis leads to chronic pancreatitis, which occurs when the pancreas is persistently inflamed. Chronic pancreatitis usually develops by early adulthood in affected individuals. Signs and symptoms of chronic pancreatitis include occasional or frequent abdominal pain of varying severity, flatulence, and bloating. Many individuals with hereditary pancreatitis also develop abnormal calcium deposits in the pancreas (pancreatic calcifications) by early adulthood.<br /><br />Years of inflammation damage the pancreas, causing the formation of scar tissue (fibrosis) in place of functioning pancreatic tissue. Pancreatic fibrosis leads to the loss of pancreatic function in many affected individuals. This loss of function can impair the production of digestive enzymes and disrupt normal digestion, leading to fatty stool (steatorrhea), weight loss, and protein and vitamin deficiencies. Because of a decrease in insulin production due to a loss of pancreatic function, about a quarter of individuals with hereditary pancreatitis will develop type 1 diabetes mellitus by mid-adulthood; the risk of developing diabetes increases with age.<br /><br />Chronic pancreatic inflammation and damage to the pancreas increase the risk of developing pancreatic cancer. The risk is particularly high in people with hereditary pancreatitis who also smoke, use alcohol, have type 1 diabetes mellitus, or have a family history of cancer. In affected individuals who develop pancreatic cancer, it is typically diagnosed in mid-adulthood.<br /><br />Complications from pancreatic cancer and type 1 diabetes mellitus are the most common causes of death in individuals with hereditary pancreatitis, although individuals with this condition are thought to have a normal life expectancy. <a target="_blank" href="https://medlineplus.gov/genetics/condition/hereditary-pancreatitis">https://medlineplus.gov/genetics/condition/hereditary-pancreatitis</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_102">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_features">Clinical features</h1><a sid="102" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat"><strong>From HPO</strong><br />
|
||
<div class="divPopper rprt" id="clin_7803"><div><strong>Abdominal pain</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>7803</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0000737</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Sign or Symptom</dd></dl></div></div></div>
|
||
<div class="spaceAbove">An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) and perceived to originate in the abdomen.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/7803">Feature record</a> | <a href="/medgen?term=%22Abdominal%20pain%22%5BClinical%20Features%5D%20OR%207803%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_18280"><div><strong>Pancreatic pseudocyst</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>18280</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0030299</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Cyst-like space not lined by epithelium and contained within the pancreas. Pancreatic pseudocysts are often associated with pancreatitis.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/18280">Feature record</a> | <a href="/medgen?term=%22Pancreatic%20pseudocyst%22%5BClinical%20Features%5D%20OR%2018280%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_20948"><div><strong>Steatorrhea</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>20948</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0038238</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Greater than normal amounts of fat in the feces. This is a result of malabsorption of lipids in the small intestine and results in frothy foul-smelling fecal matter that floats.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/20948">Feature record</a> | <a href="/medgen?term=%22Steatorrhea%22%5BClinical%20Features%5D%20OR%2020948%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_75647"><div><strong>Exocrine pancreatic insufficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75647</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0267963</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Impaired function of the exocrine pancreas associated with a reduced ability to digest foods because of lack of digestive enzymes.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/75647">Feature record</a> | <a href="/medgen?term=%22Exocrine%20pancreatic%20insufficiency%22%5BClinical%20Features%5D%20OR%2075647%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_330843"><div><strong>Pancreatic calcification</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>330843</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C1842406</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The presence of abnormal calcium deposition lesions in the pancreas.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/330843">Feature record</a> | <a href="/medgen?term=%22Pancreatic%20calcification%22%5BClinical%20Features%5D%20OR%20330843%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_871247"><div><strong>Abnormal thrombosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>871247</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C4025731</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Anatomical Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Venous or arterial thrombosis (formation of blood clots) of spontaneous nature and which cannot be fully explained by acquired risk (e.g. atherosclerosis).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/871247">Feature record</a> | <a href="/medgen?term=%22Abnormal%20thrombosis%22%5BClinical%20Features%5D%20OR%20871247%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_10805"><div><strong>Pleural effusion</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>10805</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0032227</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Pathologic Function</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The presence of an excessive amount of fluid in the pleural cavity.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/10805">Feature record</a> | <a href="/medgen?term=%22Pleural%20effusion%22%5BClinical%20Features%5D%20OR%2010805%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_14586"><div><strong>Pancreatitis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>14586</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0030305</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The presence of inflammation in the pancreas.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/14586">Feature record</a> | <a href="/medgen?term=%22Pancreatitis%22%5BClinical%20Features%5D%20OR%2014586%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_8350"><div><strong>Diabetes mellitus</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>8350</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0011849</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A group of abnormalities characterized by hyperglycemia and glucose intolerance.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/8350">Feature record</a> | <a href="/medgen?term=%22Diabetes%20mellitus%22%5BClinical%20Features%5D%20OR%208350%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_5169"><div><strong>Fever</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>5169</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0015967</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Sign or Symptom</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Body temperature elevated above the normal range.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/5169">Feature record</a> | <a href="/medgen?term=%22Fever%22%5BClinical%20Features%5D%20OR%205169%5Buid%5D">Search on this feature</a></div></div><div class="TreeLite" data-jigconfig="closed: 1"><div class="concept-def"><a class="small" href="#" onclick="jQuery(".TreeLite","#ID_102").TreeLite().openAll(); return false;">Show all</a><a class="small" href="#" onclick="jQuery(".TreeLite","#ID_102").TreeLite().closeAll(); return false;">Hide all</a></div><ul><li><span class="TLline">Abnormality of blood and blood-forming tissues</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_871247" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Abnormal thrombosis</a></span></li></ul></li><li><span class="TLline">Abnormality of metabolism/homeostasis</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_8350" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Diabetes mellitus</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_5169" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Fever</a></span></li></ul></li><li><span class="TLline">Abnormality of the digestive system</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_75647" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Exocrine pancreatic insufficiency</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_330843" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pancreatic calcification</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_18280" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pancreatic pseudocyst</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_20948" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Steatorrhea</a></span></li></ul></li><li><span class="TLline">Abnormality of the immune system</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_14586" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pancreatitis</a></span></li></ul></li><li><span class="TLline">Abnormality of the respiratory system</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_10805" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Pleural effusion</a></span></li></ul></li><li><span class="TLline">Constitutional symptom</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_7803" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Abdominal pain</a></span></li></ul></li></ul></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_118">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0238339[DISCUI]&test_type=Clinical" ref="ncbi_uid=116056">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=116056" target="_blank" href="/omim/167800">O</a></span><span class="chiclet Gcolor" title="GeneReviews"><a target="_blank" href="/books/?term=(NBK84399%20OR%20NBK190101)%20AND%20gene%5Bbook%5D&showtype=onebook" ref="ncbi_uid=116056">G</a></span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=116056" ref="ncbi_uid=116056">V</a></span></span><span class="TLline">Hereditary pancreatitis</span><ul><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1969419[DISCUI]&test_type=Clinical&redirect=true" ref="ncbi_uid=409826">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=409826" target="_blank" href="/omim/167800">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=409826" ref="ncbi_uid=409826">V</a></span></span><span class="TLline"><a href="/medgen/409826" ref="tree=GTR&ncbi_uid=409826&link_uid=409826" title="View MedGen record for 'Pancreatitis, chronic, susceptibility to'">Pancreatitis, chronic, susceptibility to</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1842402[DISCUI]&test_type=Clinical" ref="ncbi_uid=334069">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=334069" target="_blank" href="/omim/167790">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=334069" ref="ncbi_uid=334069">V</a></span></span><span class="TLline"><a href="/medgen/334069" ref="tree=GTR&ncbi_uid=334069&link_uid=334069" title="View MedGen record for 'Tropical pancreatitis'">Tropical pancreatitis</a></span></li></ul></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/18325" ref="tree=MeSH" title="MedGen record for Pathological process">Pathological process</a></span><ul><li><span class="TLline"><a href="/medgen/4347" ref="tree=MeSH" title="MedGen record for Disease">Disease</a></span><ul><li><span class="TLline"><a href="/medgen/232130" ref="tree=MeSH" title="MedGen record for Disorder by Site">Disorder by Site</a></span><ul><li><span class="TLline"><a href="/medgen/4043" ref="tree=MeSH" title="MedGen record for Disorder of endocrine system">Disorder of endocrine system</a></span><ul><li><span class="TLline"><a href="/medgen/8350" ref="tree=MeSH" title="MedGen record for Diabetes mellitus">Diabetes mellitus</a></span><ul><li><span class="TLline"><a href="/medgen/1392102" ref="tree=MeSH" title="MedGen record for Monogenic diabetes">Monogenic diabetes</a></span><ul><li><span class="matched_ds">Hereditary pancreatitis</span><ul><li><span class="TLline"><a href="/medgen/409826" ref="tree=MeSH" title="MedGen record for Pancreatitis, chronic, susceptibility to">Pancreatitis, chronic, susceptibility to</a></span></li><li><span class="TLline"><a href="/medgen/334069" ref="tree=MeSH" title="MedGen record for Tropical pancreatitis">Tropical pancreatitis</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34798985">Genetic Evaluation of Pancreatitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fu Y,
|
||
Lucas AL</span><br />
|
||
<span class="medgenPMjournal">Gastrointest Endosc Clin N Am</span>
|
||
2022 Jan;32(1):27-43.
|
||
doi: 10.1016/j.giec.2021.08.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34798985" target="_blank">34798985</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31672839">Management of patients with increased risk for familial pancreatic cancer: updated recommendations from the International Cancer of the Pancreas Screening (CAPS) Consortium.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Goggins M,
|
||
Overbeek KA,
|
||
Brand R,
|
||
Syngal S,
|
||
Del Chiaro M,
|
||
Bartsch DK,
|
||
Bassi C,
|
||
Carrato A,
|
||
Farrell J,
|
||
Fishman EK,
|
||
Fockens P,
|
||
Gress TM,
|
||
van Hooft JE,
|
||
Hruban RH,
|
||
Kastrinos F,
|
||
Klein A,
|
||
Lennon AM,
|
||
Lucas A,
|
||
Park W,
|
||
Rustgi A,
|
||
Simeone D,
|
||
Stoffel E,
|
||
Vasen HFA,
|
||
Cahen DL,
|
||
Canto MI,
|
||
Bruno M;
|
||
International Cancer of the Pancreas Screening (CAPS) consortium</span><br />
|
||
<span class="medgenPMjournal">Gut</span>
|
||
2020 Jan;69(1):7-17.
|
||
Epub 2019 Oct 31
|
||
doi: 10.1136/gutjnl-2019-319352.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31672839" target="_blank">31672839</a><a href="/pmc/articles/PMC7295005" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31860051">Diagnosis and Management of Chronic Pancreatitis: A Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Singh VK,
|
||
Yadav D,
|
||
Garg PK</span><br />
|
||
<span class="medgenPMjournal">JAMA</span>
|
||
2019 Dec 24;322(24):2422-2434.
|
||
doi: 10.1001/jama.2019.19411.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31860051" target="_blank">31860051</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22hereditary%20pancreatitis%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (28)</a></div><h3 class="subhead">Curated<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpCurated"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3><h3 class="nl vspace"><a href="https://www.nice.org.uk/guidance/ng104" target="_blank">UK NICE Guideline NG104, Pancreatitis, 2020</a></h3>
|
||
</div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34002083">Pancreatic cancer epidemiology: understanding the role of lifestyle and inherited risk factors.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Klein AP</span><br />
|
||
<span class="medgenPMjournal">Nat Rev Gastroenterol Hepatol</span>
|
||
2021 Jul;18(7):493-502.
|
||
Epub 2021 May 17
|
||
doi: 10.1038/s41575-021-00457-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34002083" target="_blank">34002083</a><a href="/pmc/articles/PMC9265847" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31672839">Management of patients with increased risk for familial pancreatic cancer: updated recommendations from the International Cancer of the Pancreas Screening (CAPS) Consortium.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Goggins M,
|
||
Overbeek KA,
|
||
Brand R,
|
||
Syngal S,
|
||
Del Chiaro M,
|
||
Bartsch DK,
|
||
Bassi C,
|
||
Carrato A,
|
||
Farrell J,
|
||
Fishman EK,
|
||
Fockens P,
|
||
Gress TM,
|
||
van Hooft JE,
|
||
Hruban RH,
|
||
Kastrinos F,
|
||
Klein A,
|
||
Lennon AM,
|
||
Lucas A,
|
||
Park W,
|
||
Rustgi A,
|
||
Simeone D,
|
||
Stoffel E,
|
||
Vasen HFA,
|
||
Cahen DL,
|
||
Canto MI,
|
||
Bruno M;
|
||
International Cancer of the Pancreas Screening (CAPS) consortium</span><br />
|
||
<span class="medgenPMjournal">Gut</span>
|
||
2020 Jan;69(1):7-17.
|
||
Epub 2019 Oct 31
|
||
doi: 10.1136/gutjnl-2019-319352.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31672839" target="_blank">31672839</a><a href="/pmc/articles/PMC7295005" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31860051">Diagnosis and Management of Chronic Pancreatitis: A Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Singh VK,
|
||
Yadav D,
|
||
Garg PK</span><br />
|
||
<span class="medgenPMjournal">JAMA</span>
|
||
2019 Dec 24;322(24):2422-2434.
|
||
doi: 10.1001/jama.2019.19411.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31860051" target="_blank">31860051</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30660731">Genetics, Cell Biology, and Pathophysiology of Pancreatitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mayerle J,
|
||
Sendler M,
|
||
Hegyi E,
|
||
Beyer G,
|
||
Lerch MM,
|
||
Sahin-Tóth M</span><br />
|
||
<span class="medgenPMjournal">Gastroenterology</span>
|
||
2019 May;156(7):1951-1968.e1.
|
||
Epub 2019 Jan 18
|
||
doi: 10.1053/j.gastro.2018.11.081.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30660731" target="_blank">30660731</a><a href="/pmc/articles/PMC6903413" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10323357">Childhood pancreatitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Uretsky G,
|
||
Goldschmiedt M,
|
||
James K</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
1999 May 1;59(9):2507-12.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10323357" target="_blank">10323357</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hereditary%20pancreatitis%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (223)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39880528">Pancreatic Cancer: Screening and Early Detection.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mohamed G,
|
||
Munir M,
|
||
Rai A,
|
||
Gaddam S</span><br />
|
||
<span class="medgenPMjournal">Gastroenterol Clin North Am</span>
|
||
2025 Mar;54(1):205-221.
|
||
Epub 2024 Nov 7
|
||
doi: 10.1016/j.gtc.2024.09.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39880528" target="_blank">39880528</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34065437">Genetic Risk Factors in Early-Onset Nonalcoholic Chronic Pancreatitis: An Update.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wertheim-Tysarowska K,
|
||
Oracz G,
|
||
Rygiel AM</span><br />
|
||
<span class="medgenPMjournal">Genes (Basel)</span>
|
||
2021 May 20;12(5)
|
||
doi: 10.3390/genes12050785.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34065437" target="_blank">34065437</a><a href="/pmc/articles/PMC8160726" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34002083">Pancreatic cancer epidemiology: understanding the role of lifestyle and inherited risk factors.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Klein AP</span><br />
|
||
<span class="medgenPMjournal">Nat Rev Gastroenterol Hepatol</span>
|
||
2021 Jul;18(7):493-502.
|
||
Epub 2021 May 17
|
||
doi: 10.1038/s41575-021-00457-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34002083" target="_blank">34002083</a><a href="/pmc/articles/PMC9265847" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31672839">Management of patients with increased risk for familial pancreatic cancer: updated recommendations from the International Cancer of the Pancreas Screening (CAPS) Consortium.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Goggins M,
|
||
Overbeek KA,
|
||
Brand R,
|
||
Syngal S,
|
||
Del Chiaro M,
|
||
Bartsch DK,
|
||
Bassi C,
|
||
Carrato A,
|
||
Farrell J,
|
||
Fishman EK,
|
||
Fockens P,
|
||
Gress TM,
|
||
van Hooft JE,
|
||
Hruban RH,
|
||
Kastrinos F,
|
||
Klein A,
|
||
Lennon AM,
|
||
Lucas A,
|
||
Park W,
|
||
Rustgi A,
|
||
Simeone D,
|
||
Stoffel E,
|
||
Vasen HFA,
|
||
Cahen DL,
|
||
Canto MI,
|
||
Bruno M;
|
||
International Cancer of the Pancreas Screening (CAPS) consortium</span><br />
|
||
<span class="medgenPMjournal">Gut</span>
|
||
2020 Jan;69(1):7-17.
|
||
Epub 2019 Oct 31
|
||
doi: 10.1136/gutjnl-2019-319352.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31672839" target="_blank">31672839</a><a href="/pmc/articles/PMC7295005" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31860051">Diagnosis and Management of Chronic Pancreatitis: A Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Singh VK,
|
||
Yadav D,
|
||
Garg PK</span><br />
|
||
<span class="medgenPMjournal">JAMA</span>
|
||
2019 Dec 24;322(24):2422-2434.
|
||
doi: 10.1001/jama.2019.19411.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31860051" target="_blank">31860051</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hereditary%20pancreatitis%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (199)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31860051">Diagnosis and Management of Chronic Pancreatitis: A Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Singh VK,
|
||
Yadav D,
|
||
Garg PK</span><br />
|
||
<span class="medgenPMjournal">JAMA</span>
|
||
2019 Dec 24;322(24):2422-2434.
|
||
doi: 10.1001/jama.2019.19411.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31860051" target="_blank">31860051</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28501969">Chronic Pancreatitis: Current Status and Challenges for Prevention and Treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lew D,
|
||
Afghani E,
|
||
Pandol S</span><br />
|
||
<span class="medgenPMjournal">Dig Dis Sci</span>
|
||
2017 Jul;62(7):1702-1712.
|
||
Epub 2017 May 13
|
||
doi: 10.1007/s10620-017-4602-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28501969" target="_blank">28501969</a><a href="/pmc/articles/PMC5507364" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26878183">Hereditary Pancreatitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rivera Rivera ED,
|
||
Chugh A,
|
||
Cordova J,
|
||
Young S</span><br />
|
||
<span class="medgenPMjournal">Pediatr Ann</span>
|
||
2016 Feb;45(2):e50-3.
|
||
doi: 10.3928/00904481-20160115-01.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26878183" target="_blank">26878183</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15231857">Epidemiology and prevention of pancreatic cancer.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lowenfels AB,
|
||
Maisonneuve P</span><br />
|
||
<span class="medgenPMjournal">Jpn J Clin Oncol</span>
|
||
2004 May;34(5):238-44.
|
||
doi: 10.1093/jjco/hyh045.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15231857" target="_blank">15231857</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10872416">Preventive strategies and therapeutic options for hereditary pancreatitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gates LK Jr</span><br />
|
||
<span class="medgenPMjournal">Med Clin North Am</span>
|
||
2000 May;84(3):589-95.
|
||
doi: 10.1016/s0025-7125(05)70242-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10872416" target="_blank">10872416</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hereditary%20pancreatitis%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (40)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31860051">Diagnosis and Management of Chronic Pancreatitis: A Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Singh VK,
|
||
Yadav D,
|
||
Garg PK</span><br />
|
||
<span class="medgenPMjournal">JAMA</span>
|
||
2019 Dec 24;322(24):2422-2434.
|
||
doi: 10.1001/jama.2019.19411.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31860051" target="_blank">31860051</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30660731">Genetics, Cell Biology, and Pathophysiology of Pancreatitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mayerle J,
|
||
Sendler M,
|
||
Hegyi E,
|
||
Beyer G,
|
||
Lerch MM,
|
||
Sahin-Tóth M</span><br />
|
||
<span class="medgenPMjournal">Gastroenterology</span>
|
||
2019 May;156(7):1951-1968.e1.
|
||
Epub 2019 Jan 18
|
||
doi: 10.1053/j.gastro.2018.11.081.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30660731" target="_blank">30660731</a><a href="/pmc/articles/PMC6903413" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27926368">Genetic Syndromes with Pancreatic Manifestations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pittman ME,
|
||
Brosens LA,
|
||
Wood LD</span><br />
|
||
<span class="medgenPMjournal">Surg Pathol Clin</span>
|
||
2016 Dec;9(4):705-715.
|
||
Epub 2016 Oct 12
|
||
doi: 10.1016/j.path.2016.05.012.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27926368" target="_blank">27926368</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15231857">Epidemiology and prevention of pancreatic cancer.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lowenfels AB,
|
||
Maisonneuve P</span><br />
|
||
<span class="medgenPMjournal">Jpn J Clin Oncol</span>
|
||
2004 May;34(5):238-44.
|
||
doi: 10.1093/jjco/hyh045.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15231857" target="_blank">15231857</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10323357">Childhood pancreatitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Uretsky G,
|
||
Goldschmiedt M,
|
||
James K</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
1999 May 1;59(9):2507-12.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10323357" target="_blank">10323357</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hereditary%20pancreatitis%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (97)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39534420">Trypsin in pancreatitis: The culprit, a mediator, or epiphenomenon?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gukovskaya AS,
|
||
Lerch MM,
|
||
Mayerle J,
|
||
Sendler M,
|
||
Ji B,
|
||
Saluja AK,
|
||
Gorelick FS,
|
||
Gukovsky I</span><br />
|
||
<span class="medgenPMjournal">World J Gastroenterol</span>
|
||
2024 Nov 7;30(41):4417-4438.
|
||
doi: 10.3748/wjg.v30.i41.4417.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39534420" target="_blank">39534420</a><a href="/pmc/articles/PMC11551668" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33909107">Hereditary pancreatitis in childhood: course of disease and complications.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Prommer R,
|
||
Kienbauer M,
|
||
Kargl S,
|
||
Schöfl R</span><br />
|
||
<span class="medgenPMjournal">Wien Klin Wochenschr</span>
|
||
2021 Jul;133(13-14):669-673.
|
||
Epub 2021 Apr 28
|
||
doi: 10.1007/s00508-021-01869-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33909107" target="_blank">33909107</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31860051">Diagnosis and Management of Chronic Pancreatitis: A Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Singh VK,
|
||
Yadav D,
|
||
Garg PK</span><br />
|
||
<span class="medgenPMjournal">JAMA</span>
|
||
2019 Dec 24;322(24):2422-2434.
|
||
doi: 10.1001/jama.2019.19411.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31860051" target="_blank">31860051</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30660731">Genetics, Cell Biology, and Pathophysiology of Pancreatitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mayerle J,
|
||
Sendler M,
|
||
Hegyi E,
|
||
Beyer G,
|
||
Lerch MM,
|
||
Sahin-Tóth M</span><br />
|
||
<span class="medgenPMjournal">Gastroenterology</span>
|
||
2019 May;156(7):1951-1968.e1.
|
||
Epub 2019 Jan 18
|
||
doi: 10.1053/j.gastro.2018.11.081.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30660731" target="_blank">30660731</a><a href="/pmc/articles/PMC6903413" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10982192">Origin and implication of the hereditary pancreatitis-associated N21I mutation in the cationic trypsinogen gene.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chen JM,
|
||
Ferec C</span><br />
|
||
<span class="medgenPMjournal">Hum Genet</span>
|
||
2000 Jan;106(1):125-6.
|
||
doi: 10.1007/s004390051019.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10982192" target="_blank">10982192</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hereditary%20pancreatitis%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (88)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/35142721">Chronic Pancreatitis Is a Risk Factor for Pancreatic Cancer, and Incidence Increases With Duration of Disease: A Systematic Review and Meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gandhi S,
|
||
de la Fuente J,
|
||
Murad MH,
|
||
Majumder S</span><br />
|
||
<span class="medgenPMjournal">Clin Transl Gastroenterol</span>
|
||
2022 Mar 28;13(3):e00463.
|
||
doi: 10.14309/ctg.0000000000000463.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35142721" target="_blank">35142721</a><a href="/pmc/articles/PMC8963838" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32703081">Prophylactic total pancreatectomy in individuals at high risk of pancreatic ductal adenocarcinoma (PROPAN): systematic review and shared decision-making programme using decision tables.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Scholten L,
|
||
Latenstein AE,
|
||
Aalfs CM,
|
||
Bruno MJ,
|
||
Busch OR,
|
||
Bonsing BA,
|
||
Koerkamp BG,
|
||
Molenaar IQ,
|
||
Ubbink DT,
|
||
van Hooft JE,
|
||
Fockens P,
|
||
Glas J,
|
||
DeVries JH,
|
||
Besselink MG;
|
||
Dutch Pancreatic Cancer Group</span><br />
|
||
<span class="medgenPMjournal">United European Gastroenterol J</span>
|
||
2020 Oct;8(8):865-877.
|
||
Epub 2020 Jul 23
|
||
doi: 10.1177/2050640620945534.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32703081" target="_blank">32703081</a><a href="/pmc/articles/PMC7707864" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25479908">High-risk population in sporadic pancreatic adenocarcinoma: guidelines for screening.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bruenderman EH,
|
||
Martin RC 2nd</span><br />
|
||
<span class="medgenPMjournal">J Surg Res</span>
|
||
2015 Mar;194(1):212-9.
|
||
Epub 2014 Oct 13
|
||
doi: 10.1016/j.jss.2014.06.046.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25479908" target="_blank">25479908</a><a href="/pmc/articles/PMC4559279" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22543443">Acute pancreatitis in pediatrics: a systematic review of the literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mekitarian Filho E,
|
||
Carvalho WB,
|
||
Silva FD</span><br />
|
||
<span class="medgenPMjournal">J Pediatr (Rio J)</span>
|
||
2012 Mar-Apr;88(2):101-14.
|
||
doi: 10.2223/JPED.2163.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22543443" target="_blank">22543443</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Hereditary%20pancreatitis%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (4)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
</div>
|
||
<div class=" bottom">
|
||
|
||
</div>
|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
||
<!-- MedGen supplemental column starts here -->
|
||
<div class="rightCol mgCol">
|
||
<div class="portlet mgSection" id="ID_113">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul id="my-toc"></ul></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_106">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Genetic_Testing_Registry">Genetic Testing Registry</h1><a sid="106" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C0238339%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (89)</a></li>
|
||
<li><a href="/gtr/tests?term=C0238339%5bDISCUI%5d&filter=method%3A2%5F12" target="_blank">Microsatellite instability testing (MSI) (1)</a></li>
|
||
<li><a href="/gtr/tests?term=C0238339%5bDISCUI%5d&filter=method%3A2%5F18" target="_blank">Mutation scanning of select exons (2)</a></li>
|
||
<li><a href="/gtr/tests?term=C0238339%5bDISCUI%5d&filter=method%3A2%5F17" target="_blank">Mutation scanning of the entire coding region (3)</a></li>
|
||
<li><a href="/gtr/tests?term=C0238339%5bDISCUI%5d&filter=method%3A2%5F9" target="_blank">Sequence analysis of select exons (7)</a></li>
|
||
<li><a href="/gtr/tests?term=C0238339%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (117)</a></li>
|
||
<li><a href="/gtr/tests?term=C0238339%5bDISCUI%5d&filter=method%3A2%5F19" target="_blank">Targeted variant analysis (19)</a></li>
|
||
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C0238339%5bDISCUI%5d" target="_blank">See all (143)</a></total></li>
|
||
</ul></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_119">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_resources">Clinical resources</h1><a sid="119" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul><li><a href="https://www.omim.org/search?index=entry&start=1&limit=10&sort=score%20desc&field=number&search=167800" target="_blank">OMIM</a></li><li><a href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=676" target="_blank">Orphanet</a></li><li><a href="https://clinicaltrials.gov/search?cond=Hereditary%20pancreatitis" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_121">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22hereditary%20pancreatitis%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Hereditary%20pancreatitis%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul><h3 class="subhead">Curated</h3><ul class="a_poppers"><li><a target="_blank" href="https://www.nice.org.uk/guidance/ng104">NICE, 2020</a><div>UK NICE Guideline NG104, Pancreatitis, 2020</div></li></ul></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_115">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Molecular_resources">Molecular resources</h1><a sid="115" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul><li><a href="http://www.omim.org/search?index=entry&start=1&limit=10&sort=score%20desc&field=number&search=167790%20276000%20601405%20601564%20602421" target="_blank">OMIM</a></li><li><a href="/clinvar/?term=1080[geneid]" target="_blank">View CFTR variations in ClinVar</a></li><li><a href="/clinvar/?term=5644[geneid]" target="_blank">View PRSS1 variations in ClinVar</a></li><li><a href="/clinvar/?term=5645[geneid]" target="_blank">View PRSS2 variations in ClinVar</a></li><li><a href="/clinvar/?term=6690[geneid]" target="_blank">View SPINK1 variations in ClinVar</a></li><li><a href="/clinvar/?term=11330[geneid]" target="_blank">View CTRC variations in ClinVar</a></li><li><a href="/nuccore/195539334,196115071,219521921,287325315,312839845" target="_blank">RefSeqGene</a></li><li><a href="https://catalog.coriell.org/Search?q=167800" target="_blank">Coriell Institute for Medical Research</a></li></ul></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_116">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Consumer_resources">Consumer resources</h1><a sid="116" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul><li><a href="https://www.malacards.org/card/pancreatitis_hereditary" target="_blank">MalaCards</a></li><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Hereditary%20pancreatitis" target="_blank">MedlinePlus</a></li><li><a href="https://medlineplus.gov/genetics/condition/hereditary-pancreatitis" target="_blank">MedlinePlusGenetics (GHR)</a></li><li><a href="https://rarediseases.info.nih.gov/diseases/6632/disease" target="_blank">NCATS Office of Rare Diseases Research (GARD)</a></li></ul></div>
|
||
</div>
|
||
</div>
|
||
<div class="portlet brieflink">
|
||
<div class="portlet_head">
|
||
<div class="portlet_title">
|
||
<h3>Reviews</h3>
|
||
</div>
|
||
<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.MedGen_SingleItemSuplCluster.MedGenReviews.Shutter" sid="1" href="#" class="portlet_shutter" title="Show/hide content" remembercollapsed="true" pgsec_name="Reviews" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.MedGen_SingleItemSuplCluster.MedGenReviews.Shutter"></a>
|
||
</div>
|
||
<div class="portlet_content">
|
||
<ul>
|
||
<li>
|
||
<a href="/pubmed/22379635" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=4" target="_blank"><span class="gene_reviews">GeneReviews</span></a>
|
||
</li>
|
||
<li>
|
||
<a href="/pubmed/24624459" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=4" target="_blank"><span class="gene_reviews">GeneReviews</span></a>
|
||
</li>
|
||
<li>
|
||
<a href="/pubmed/clinical?term=Hereditary%20pancreatitis" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=3&linkpostotal=4" target="_blank">PubMed Clinical Queries</a>
|
||
</li>
|
||
<li>
|
||
<a href="/pubmed?term=Hereditary%20pancreatitis%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=4&linkpostotal=4" target="_blank">Reviews in PubMed</a>
|
||
</li>
|
||
</ul>
|
||
</div>
|
||
</div>
|
||
|
||
<!-- MedGen supplemental column ends here -->
|
||
<div class="portlet brieflink">
|
||
<div class="portlet_head">
|
||
<div class="portlet_title">
|
||
<h3>Related information</h3>
|
||
</div>
|
||
<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.MedGen_SingleItemSuplCluster.MedGenDiscoveryDbLinks.Shutter" sid="1" href="#" class="portlet_shutter" title="Show/hide content" remembercollapsed="true" pgsec_name="discovery_db_links" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.MedGen_SingleItemSuplCluster.MedGenDiscoveryDbLinks.Shutter"></a>
|
||
</div>
|
||
<div class="portlet_content DiscoveryDbLinks">
|
||
<ul>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/clinvar?LinkName=medgen_clinvar&from_uid=116056" ref="log$=recordlinks">ClinVar</a>
|
||
<div class="brieflinkpop offscreen_noflow">Related medical variations</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/gene?LinkName=medgen_gene_diseases&from_uid=116056" ref="log$=recordlinks">Gene</a>
|
||
<div class="brieflinkpop offscreen_noflow">Related information in NCBI Gene</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/gtr/tests?term=C0238339[DISCUI]" ref="log$=recordlinks">GTR</a>
|
||
<div class="brieflinkpop offscreen_noflow">Related information in GTR</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/gtr/tests?term=C0238339[DISCUI]&test_type=Clinical" ref="log$=recordlinks">GTR(Clinical)</a>
|
||
<div class="brieflinkpop offscreen_noflow">Clinical tests in GTR</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/mesh?LinkName=medgen_mesh&from_uid=116056" ref="log$=recordlinks">MeSH</a>
|
||
<div class="brieflinkpop offscreen_noflow">Related Medical Subject Headings</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/omim?LinkName=medgen_omim&from_uid=116056" ref="log$=recordlinks">OMIM</a>
|
||
<div class="brieflinkpop offscreen_noflow">Related records in OMIM</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/omim?LinkName=medgen_omim_gene&from_uid=116056" ref="log$=recordlinks">OMIM(Genes)</a>
|
||
<div class="brieflinkpop offscreen_noflow">OMIM records containing genes associated with phenotypes registered in MedGen</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/pmc?LinkName=medgen_pmc&from_uid=116056" ref="log$=recordlinks">PMC Articles</a>
|
||
<div class="brieflinkpop offscreen_noflow">Related information in PubMed Central Links</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed&from_uid=116056" ref="log$=recordlinks">PubMed</a>
|
||
<div class="brieflinkpop offscreen_noflow">Related literature resources in PubMed</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed_bookshelf_cited&from_uid=116056" ref="log$=recordlinks">PubMed (Bookshelf cited)</a>
|
||
<div class="brieflinkpop offscreen_noflow">Links to PubMed based on citations in GeneReviews and Medical Genetics Summaries</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed_genereviews&from_uid=116056" ref="log$=recordlinks">PubMed (GeneReviews)</a>
|
||
<div class="brieflinkpop offscreen_noflow">GeneReviews in PubMed</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed_omim&from_uid=116056" ref="log$=recordlinks">PubMed (OMIM)</a>
|
||
<div class="brieflinkpop offscreen_noflow">Related literature resources in PubMed</div>
|
||
</li>
|
||
</ul>
|
||
</div>
|
||
</div>
|
||
|
||
|
||
<div class="portlet">
|
||
<div class="portlet_head">
|
||
<div class="portlet_title">
|
||
<h3>Recent activity</h3>
|
||
</div>
|
||
<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.Shutter" sid="1" href="#" class="portlet_shutter" title="Show/hide content" remembercollapsed="true" pgsec_name="recent_activity" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.Shutter"></a>
|
||
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|
||
<div class="portlet_content">
|
||
<div id="HTDisplay" class="">
|
||
<input name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.Cmd" sid="1" type="hidden" />
|
||
<div class="action">
|
||
<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory" sid="1" realname="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory" cmd="ClearHT" href="?cmd=ClearHT&" onclick="return false;" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory">
|
||
Clear
|
||
</a>
|
||
<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle" sid="1" realname="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle" class="HTOn" cmd="HTOff" href="?cmd=HTOff&" onclick="return false;" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle">
|
||
Turn Off
|
||
</a>
|
||
<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle" sid="2" realname="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle" class="HTOff" cmd="HTOn" href="?cmd=HTOn&" onclick="return false;" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.HistoryToggle">
|
||
Turn On
|
||
</a>
|
||
</div>
|
||
<ul id="activity">
|
||
<li class="ra_rcd ralinkpopper two_line">
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