Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormality of the upper urinary tract (HP:0010935)

Parent Node:
Abnormality of the ureter (HP:0000069)

..Starting node
..Ureteral dysgenesis (HP:0008631)

Term ID:

8631

Name:

Ureteral dysgenesis

Synonym:

Definition:

A developmental anomaly of the ureter.

Comments:

Reference:

HP:0008631

Genes and Diseases:

Child Nodes:

Sister Nodes:

Congenital megaureter (HP:0008676)

Hydroureter (HP:0000072)

Neoplasm of the ureter (HP:0100516)

Ureteral agenesis (HP:0012300)

Ureteral atresia (HP:0005999)

Ureteral duplication (HP:0000073)

Ureteral obstruction (HP:0006000)

Ureterocele (HP:0000070)

Vesicoureteral reflux (HP:0000076)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008631	HP:0008631	Ureteral dysgenesis	0	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.