Human Phenotype Ontology 
Grandparent Node:
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Phenotypic abnormality (HP:0000118)help
Parent Node:
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Abdominal wall defect (HP:0010866)help
Parent Node:
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Abnormality of the genitourinary system (HP:0000119)help
..Starting node
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Cloacal abnormality (HP:0012620)help
Term ID: 12620
Name: Cloacal abnormality
Synonym:
Definition: A developmental anomaly associated with the failure of rectum, vagina, and bladder to separate.
Comments:
Reference: HP:0012620
Genes and Diseases:
 
       Child Nodes:
........expandCloacal exstrophy (HP:0010475) help
........expandPersistent cloaca (HP:0012621) help

 Sister Nodes: 
..expandAbnormality of the genital system (HP:0000078) help
..expandAbnormality of the urinary system (HP:0000079) help
..expandNeoplasm of the genitourinary tract (HP:0007379) help
..expandUrogenital fistula (HP:0100589) 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:0012620HP:0012620Cloacal abnormality0 CL E G H
HP:0012620HP:0012621Persistent cloaca1 CL E G H
HP:0012620HP:0010475Cloacal exstrophy1 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.