Human Phenotype Ontology 
Grandparent Node:
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Abnormal intestine morphology (HP:0002242)help
Parent Node:
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Abnormality of intestinal smooth muscle morphology (HP:0030935)help
..Starting node
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Abnormal layering of muscularis propria (HP:0030936)help
Term ID: 30936
Name: Abnormal layering of muscularis propria
Synonym: Muscularis propria malformation; Segmental additional circular muscle coat
Definition: Abnormal layering of the intestinal muscularis propria into three layers; (1) inner circular; (2) additional oblique; and (3) outer longitudinal layer.
Comments:
Reference: HP:0030936
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAtrophic muscularis propria (HP:0025149) help
..expandFibrotic muscularis propria (HP:0030937) 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:0030936HP:0030936Abnormal layering of muscularis propria0 CL E G H


Genes (0) :

Diseases (0) :
 

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