Human Phenotype Ontology 
Grandparent Node:
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Abnormal gastrointestinal motility (HP:0030895)help
Parent Node:
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Abnormality of the small intestine (HP:0002244)help
Parent Node:
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Gastrointestinal dysmotility (HP:0002579)help
..Starting node
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Small intestinal dysmotility (HP:0012850)help
Term ID: 12850
Name: Small intestinal dysmotility
Synonym:
Definition: Abnormal small intestinal contractions, such as spasms and intestinal paralysis related to the loss of the ability of the gut to coordinate muscular activity because of endogenous or exogenous causes.
Comments:
Reference: HP:0012850
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal peristalsis (HP:0030914) help
..expandIleus (HP:0002595) help
..expandIntestinal pseudo-obstruction (HP:0004389) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0012850HP:0012850Small intestinal dysmotility0POLG CL E G H5428298Mitochondrial neurogastrointestinal encephalomyopathyCN918676ORPHA123249179174763
HP:0012850HP:0012850Small intestinal dysmotility0RRM2B CL E G H50484298Mitochondrial neurogastrointestinal encephalomyopathyCN918676ORPHA135417296604712
HP:0012850HP:0012850Small intestinal dysmotility0TYMP CL E G H1890298Mitochondrial neurogastrointestinal encephalomyopathyCN918676ORPHA18953148131222
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (3) :POLG RRM2B TYMP

Diseases (1) :298
 

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