Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the upper urinary tract (HP:0010935)help
Parent Node:
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Abnormality of the ureter (HP:0000069)help
..Starting node
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Ureteral agenesis (HP:0012300)help
Term ID: 12300
Name: Ureteral agenesis
Synonym:
Definition: Failure of the ureter to undergo development.
Comments:
Reference: HP:0012300
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCongenital megaureter (HP:0008676) help
..expandHydroureter (HP:0000072) help
..expandNeoplasm of the ureter (HP:0100516) help
..expandUreteral atresia (HP:0005999) help
..expandUreteral duplication (HP:0000073) help
..expandUreteral dysgenesis (HP:0008631) help
..expandUreteral obstruction (HP:0006000) help
..expandUreterocele (HP:0000070) help
..expandVesicoureteral reflux (HP:0000076) 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:0012300HP:0012300Ureteral agenesis0CEP55 CL E G H551651161OMIM:236500Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly2


Genes (1) :CEP55

Diseases (1) :OMIM:236500
 

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