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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100771HP:0100771Hypoperistalsis0AAAS CL E G H808613666OMIM:231550Achalasia-Addisonianism-Alacrima syndrome57
HP:0100771HP:0100771Hypoperistalsis0AAAS CL E G H808613666ORPHA:869Triple A syndrome57
HP:0100771HP:0100771Hypoperistalsis0ACTA2 CL E G H59130OMIM:613834Multisystemic smooth muscle dysfunction syndrome94
HP:0100771HP:0100771Hypoperistalsis0ACTB CL E G H60132ORPHA:79107Developmental malformations-deafness-dystonia syndrome72
HP:0100771HP:0100771Hypoperistalsis0ACTB CL E G H60132OMIM:607371Dystonia, juvenile-onset72
HP:0100771HP:0100771Hypoperistalsis0ACTG2 CL E G H72145ORPHA:2241Megacystis-microcolon-intestinal hypoperistalsis syndromeHP:0040281 - Very frequent23
HP:0100771HP:0100771Hypoperistalsis0COL4A5 CL E G H12872207ORPHA:1018X-linked Alport syndrome-diffuse leiomyomatosisHP:0040282 - Frequent678
HP:0100771HP:0100771Hypoperistalsis0COL4A6 CL E G H12882208ORPHA:1018X-linked Alport syndrome-diffuse leiomyomatosisHP:0040282 - Frequent18
HP:0100771HP:0100771Hypoperistalsis0FLVCR1 CL E G H2898224682OMIM:609033Ataxia, posterior column, with retinitis pigmentosa111
HP:0100771HP:0100771Hypoperistalsis0GLA CL E G H27174296ORPHA:324Fabry disease291
HP:0100771HP:0100771Hypoperistalsis0GMPPA CL E G H2992622923OMIM:615510Alacrima, achalasia, and mental retardation syndrome24
HP:0100771HP:0100771Hypoperistalsis0GMPPA CL E G H2992622923ORPHA:869Triple A syndrome24
HP:0100771HP:0100771Hypoperistalsis0GUCY1A1 CL E G H29824685OMIM:615750Moyamoya disease 6 with achalasia
HP:0100771HP:0100771Hypoperistalsis0IARS2 CL E G H5569929685ORPHA:436174Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome25
HP:0100771HP:0100771Hypoperistalsis0IARS2 CL E G H5569929685OMIM:616007Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia25
HP:0100771HP:0100771Hypoperistalsis0IVNS1ABP CL E G H1062516951OMIM:618969IMMUNODEFICIENCY 70; IMD70
HP:0100771HP:0100771Hypoperistalsis0LMOD1 CL E G H258026647ORPHA:2241Megacystis-microcolon-intestinal hypoperistalsis syndromeHP:0040281 - Very frequent
HP:0100771HP:0100771Hypoperistalsis0MEIS2 CL E G H42127001OMIM:600987Cleft palate, cardiac defects, and mental retardation7
HP:0100771HP:0100771Hypoperistalsis0MYH11 CL E G H46297569ORPHA:2241Megacystis-microcolon-intestinal hypoperistalsis syndromeHP:0040281 - Very frequent418
HP:0100771HP:0100771Hypoperistalsis0MYH11 CL E G H46297569OMIM:619350VISCERAL MYOPATHY 2; VSCM2418
HP:0100771HP:0100771Hypoperistalsis0MYL9 CL E G H1039815754OMIM:619365MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 4; MMIHS4
HP:0100771HP:0100771Hypoperistalsis0MYLK CL E G H46387590ORPHA:2241Megacystis-microcolon-intestinal hypoperistalsis syndromeHP:0040281 - Very frequent326
HP:0100771HP:0100771Hypoperistalsis0MYO1H CL E G H28344613879OMIM:619482CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 2, AND AUTONOMIC DYSFUNCTION; CCHS2
HP:0100771HP:0100771Hypoperistalsis0PHOX2B CL E G H89299143OMIM:209880Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease86
HP:0100771HP:0100771Hypoperistalsis0RAD21 CL E G H58859811OMIM:611376Mungan syndrome.25
HP:0100771HP:0100771Hypoperistalsis0SAMD9 CL E G H548091348OMIM:617053Mirage syndrome8
HP:0100771HP:0100771Hypoperistalsis0STAT3 CL E G H677411364OMIM:615952AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1110
HP:0100771HP:0100771Hypoperistalsis0TRAPPC11 CL E G H6068425751OMIM:615356Muscular dystrophy, limb-girdle, autosomal recessive 1827
HP:0100771HP:0100771Hypoperistalsis0TRAPPC11 CL E G H6068425751ORPHA:869Triple A syndrome27
HP:0100771HP:0031857Ineffective esophageal peristalsis1AAAS CL E G H808613666OMIM:231550Achalasia-Addisonianism-Alacrima syndrome57
HP:0100771HP:0031857Ineffective esophageal peristalsis1AAAS CL E G H808613666ORPHA:869Triple A syndrome57
HP:0100771HP:0031857Ineffective esophageal peristalsis1ACTB CL E G H60132ORPHA:79107Developmental malformations-deafness-dystonia syndrome72
HP:0100771HP:0031857Ineffective esophageal peristalsis1ACTB CL E G H60132OMIM:607371Dystonia, juvenile-onset72
HP:0100771HP:0031857Ineffective esophageal peristalsis1COL4A5 CL E G H12872207ORPHA:1018X-linked Alport syndrome-diffuse leiomyomatosis678
HP:0100771HP:0031857Ineffective esophageal peristalsis1COL4A6 CL E G H12882208ORPHA:1018X-linked Alport syndrome-diffuse leiomyomatosis18
HP:0100771HP:0031857Ineffective esophageal peristalsis1FLVCR1 CL E G H2898224682OMIM:609033Ataxia, posterior column, with retinitis pigmentosa111
HP:0100771HP:0031857Ineffective esophageal peristalsis1GLA CL E G H27174296ORPHA:324Fabry disease291
HP:0100771HP:0031857Ineffective esophageal peristalsis1GMPPA CL E G H2992622923OMIM:615510Alacrima, achalasia, and mental retardation syndrome24
HP:0100771HP:0031857Ineffective esophageal peristalsis1GMPPA CL E G H2992622923ORPHA:869Triple A syndrome24
HP:0100771HP:0031857Ineffective esophageal peristalsis1GUCY1A1 CL E G H29824685OMIM:615750Moyamoya disease 6 with achalasia
HP:0100771HP:0031857Ineffective esophageal peristalsis1IARS2 CL E G H5569929685ORPHA:436174Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome25
HP:0100771HP:0031857Ineffective esophageal peristalsis1IARS2 CL E G H5569929685OMIM:616007Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia25
HP:0100771HP:0031857Ineffective esophageal peristalsis1IVNS1ABP CL E G H1062516951OMIM:618969IMMUNODEFICIENCY 70; IMD70
HP:0100771HP:0031857Ineffective esophageal peristalsis1MEIS2 CL E G H42127001OMIM:600987Cleft palate, cardiac defects, and mental retardation7
HP:0100771HP:0031857Ineffective esophageal peristalsis1MYH11 CL E G H46297569OMIM:619350VISCERAL MYOPATHY 2; VSCM2418
HP:0100771HP:0031857Ineffective esophageal peristalsis1MYO1H CL E G H28344613879OMIM:619482CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 2, AND AUTONOMIC DYSFUNCTION; CCHS2
HP:0100771HP:0031857Ineffective esophageal peristalsis1PHOX2B CL E G H89299143OMIM:209880Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease86
HP:0100771HP:0031857Ineffective esophageal peristalsis1SAMD9 CL E G H548091348OMIM:617053Mirage syndrome8
HP:0100771HP:0031857Ineffective esophageal peristalsis1STAT3 CL E G H677411364OMIM:615952AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1110
HP:0100771HP:0031857Ineffective esophageal peristalsis1TRAPPC11 CL E G H6068425751OMIM:615356Muscular dystrophy, limb-girdle, autosomal recessive 1827
HP:0100771HP:0031857Ineffective esophageal peristalsis1TRAPPC11 CL E G H6068425751ORPHA:869Triple A syndrome27
HP:0100771HP:0002571Achalasia2AAAS CL E G H808613666OMIM:231550Achalasia-Addisonianism-Alacrima syndrome.57
HP:0100771HP:0002571Achalasia2AAAS CL E G H808613666ORPHA:869Triple A syndromeHP:0040281 - Very frequent57
HP:0100771HP:0002571Achalasia2ACTB CL E G H60132ORPHA:79107Developmental malformations-deafness-dystonia syndromeHP:0040281 - Very frequent72
HP:0100771HP:0002571Achalasia2ACTB CL E G H60132OMIM:607371Dystonia, juvenile-onset.72
HP:0100771HP:0002571Achalasia2COL4A5 CL E G H12872207ORPHA:1018X-linked Alport syndrome-diffuse leiomyomatosisHP:0040282 - Frequent678
HP:0100771HP:0002571Achalasia2COL4A6 CL E G H12882208ORPHA:1018X-linked Alport syndrome-diffuse leiomyomatosisHP:0040282 - Frequent18
HP:0100771HP:0002571Achalasia2FLVCR1 CL E G H2898224682OMIM:609033Ataxia, posterior column, with retinitis pigmentosa.HP:0011463 - Childhood onset111
HP:0100771HP:0002571Achalasia2GLA CL E G H27174296ORPHA:324Fabry diseaseHP:0040283 - Occasional291
HP:0100771HP:0002571Achalasia2GMPPA CL E G H2992622923OMIM:615510Alacrima, achalasia, and mental retardation syndrome.24
HP:0100771HP:0002571Achalasia2GMPPA CL E G H2992622923ORPHA:869Triple A syndromeHP:0040281 - Very frequent24
HP:0100771HP:0002571Achalasia2GUCY1A1 CL E G H29824685OMIM:615750Moyamoya disease 6 with achalasia.
HP:0100771HP:0002571Achalasia2IARS2 CL E G H5569929685ORPHA:436174Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndromeHP:0040281 - Very frequent25
HP:0100771HP:0002571Achalasia2IARS2 CL E G H5569929685OMIM:616007Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia25
HP:0100771HP:0002571Achalasia2IVNS1ABP CL E G H1062516951OMIM:618969IMMUNODEFICIENCY 70; IMD70
HP:0100771HP:0002571Achalasia2MEIS2 CL E G H42127001OMIM:600987Cleft palate, cardiac defects, and mental retardation7
HP:0100771HP:0002571Achalasia2MYO1H CL E G H28344613879OMIM:619482CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 2, AND AUTONOMIC DYSFUNCTION; CCHS2
HP:0100771HP:0002571Achalasia2SAMD9 CL E G H548091348OMIM:617053Mirage syndromeHP:0040283 - Occasional8
HP:0100771HP:0002571Achalasia2STAT3 CL E G H677411364OMIM:615952AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1110
HP:0100771HP:0002571Achalasia2TRAPPC11 CL E G H6068425751OMIM:615356Muscular dystrophy, limb-girdle, autosomal recessive 18HP:0040283 - Occasional27
HP:0100771HP:0002571Achalasia2TRAPPC11 CL E G H6068425751ORPHA:869Triple A syndromeHP:0040281 - Very frequent27


Genes (23) :AAAS ACTA2 ACTB ACTG2 COL4A5 COL4A6 FLVCR1 GLA GMPPA GUCY1A1 IARS2 IVNS1ABP LMOD1 MEIS2 MYH11 MYL9 MYLK MYO1H PHOX2B RAD21 SAMD9 STAT3 TRAPPC11

Diseases (23) :OMIM:231550 ORPHA:869 OMIM:613834 ORPHA:79107 OMIM:607371 ORPHA:2241 ORPHA:1018 OMIM:609033 ORPHA:324 OMIM:615510 OMIM:615750 ORPHA:436174 OMIM:616007 OMIM:618969 OMIM:600987 OMIM:619350 OMIM:619365 OMIM:619482 OMIM:209880 OMIM:611376 OMIM:617053 OMIM:615952 OMIM:615356
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.