Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the genitourinary system (HP:0000119)help
Parent Node:
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Abnormality of the urinary system (HP:0000079)help
..Starting node
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Urinary tract atresia (HP:0000809)help
Term ID: 809
Name: Urinary tract atresia
Synonym:
Definition: Congenital absence of the normal opening of a structure of the urinary tract.
Comments:
Reference: HP:0000809
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of the lower urinary tract (HP:0010936) help
..expandAbnormality of the upper urinary tract (HP:0010935) help
..expandAbnormality of the urinary system physiology (HP:0011277) 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:0000809HP:0000809Urinary tract atresia0 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.