Human Phenotype Ontology 
Grandparent Node:
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Gastrointestinal dysmotility (HP:0002579)help
Parent Node:
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Abnormal peristalsis (HP:0030914)help
..Starting node
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Hypoperistalsis (HP:0100771)help
Term ID: 100771
Name: Hypoperistalsis
Synonym: Intestinal hypoperistalsis
Definition: Reduced or inadequate peristalsis, with resultant slow passage of contents through the digestive tract.
Comments:
Reference: HP:0100771
Genes and Diseases:
 
       Child Nodes:
........expandIneffective esophageal peristalsis (HP:0031857) help
................... HP:0002571 Achalasia

 Sister Nodes: 
..expandHyperperistalsis (HP:0100770) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0100771HP:0100771Hypoperistalsis0ACTG2 CL E G H722241Factor XI deficiency, congenitalORPHA163145102545
HP:0100771HP:0100771Hypoperistalsis0ACTG2 CL E G H722241Factor XI deficiency, congenitalORPHA167145102545
HP:0100771HP:0100771Hypoperistalsis0LMOD1 CL E G H258022241Factor XI deficiency, congenitalORPHA1316647602715
HP:0100771HP:0100771Hypoperistalsis0MYH11 CL E G H46292241Factor XI deficiency, congenitalORPHA124637569160745
HP:0100771HP:0100771Hypoperistalsis0MYH11 CL E G H46292241Factor XI deficiency, congenitalORPHA123297569160745
HP:0100771HP:0100771Hypoperistalsis0MYLK CL E G H46382241Factor XI deficiency, congenitalORPHA112087590600922
HP:0100771HP:0100771Hypoperistalsis0MYLK CL E G H46382241Factor XI deficiency, congenitalORPHA110927590600922
HP:0100771HP:0100771Hypoperistalsis0RAD21 CL E G H5885611376Mungan syndrome611376C1969653OMIM12549811606462
HP:0100771HP:0100771Hypoperistalsis0RAD21 CL E G H5885611376Mungan syndrome611376C1969653OMIM12399811606462
HP:0100771HP:0031857Ineffective esophageal peristalsis1ACTG2 CL E G H722241Factor XI deficiency, congenitalORPHA163145102545
HP:0100771HP:0031857Ineffective esophageal peristalsis1ACTG2 CL E G H722241Factor XI deficiency, congenitalORPHA167145102545
HP:0100771HP:0031857Ineffective esophageal peristalsis1LMOD1 CL E G H258022241Factor XI deficiency, congenitalORPHA1316647602715
HP:0100771HP:0031857Ineffective esophageal peristalsis1MYH11 CL E G H46292241Factor XI deficiency, congenitalORPHA124637569160745
HP:0100771HP:0031857Ineffective esophageal peristalsis1MYH11 CL E G H46292241Factor XI deficiency, congenitalORPHA123297569160745
HP:0100771HP:0031857Ineffective esophageal peristalsis1MYLK CL E G H46382241Factor XI deficiency, congenitalORPHA112087590600922
HP:0100771HP:0031857Ineffective esophageal peristalsis1MYLK CL E G H46382241Factor XI deficiency, congenitalORPHA110927590600922
HP:0100771HP:0031857Ineffective esophageal peristalsis1RAD21 CL E G H5885611376Mungan syndrome611376C1969653OMIM12549811606462
HP:0100771HP:0031857Ineffective esophageal peristalsis1RAD21 CL E G H5885611376Mungan syndrome611376C1969653OMIM12399811606462
HP:0100771HP:0002571Achalasia2ACTG2 CL E G H722241Factor XI deficiency, congenitalORPHA167145102545
HP:0100771HP:0002571Achalasia2ACTG2 CL E G H722241Factor XI deficiency, congenitalORPHA163145102545
HP:0100771HP:0002571Achalasia2LMOD1 CL E G H258022241Factor XI deficiency, congenitalORPHA1316647602715
HP:0100771HP:0002571Achalasia2MYH11 CL E G H46292241Factor XI deficiency, congenitalORPHA124637569160745
HP:0100771HP:0002571Achalasia2MYH11 CL E G H46292241Factor XI deficiency, congenitalORPHA123297569160745
HP:0100771HP:0002571Achalasia2MYLK CL E G H46382241Factor XI deficiency, congenitalORPHA112087590600922
HP:0100771HP:0002571Achalasia2MYLK CL E G H46382241Factor XI deficiency, congenitalORPHA110927590600922
HP:0100771HP:0002571Achalasia2RAD21 CL E G H5885611376Mungan syndrome611376C1969653OMIM12399811606462
HP:0100771HP:0002571Achalasia2RAD21 CL E G H5885611376Mungan syndrome611376C1969653OMIM12549811606462
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (18) :AAAS ACTB ACTG2 CRLF1 FLVCR1 GLA GMPPA GUCY1A1 HLA-DQA1 HLA-DQB1 IARS2 LMOD1 MYH11 MYLK NOS1 RAD21 SAMD9 TRAPPC11

Diseases (14) :2241 611376 869 231550 79107 607371 930 609033 324 615510 615750 436174 617053 615356
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.