Human Phenotype Ontology

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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:
Abnormal renal morphology (HP:0012210)

Parent Node:
Renal atrophy (HP:0012585)

..Starting node
..Unilateral renal atrophy (HP:0008717)

Term ID:

8717

Name:

Unilateral renal atrophy

Synonym:

Kidney degeneration on one side; Unilateral kidney wasting

Definition:

A unilateral form of atrophy of the kidney.

Comments:

Reference:

HP:0008717

Genes and Diseases:

Child Nodes:

Sister Nodes:

Bilateral renal atrophy (HP:0012586)

Renal cortical atrophy (HP:0002048)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008717	HP:0008717	Unilateral renal atrophy	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.