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:
Abnormal localization of kidney (HP:0100542)

..Starting node
..Nephroptosis (HP:0011126)

Term ID:

11126

Name:

Nephroptosis

Synonym:

Floating kidney; Renal ptosis

Definition:

A significant descent of the kidney as the patient moves from the supine to the erect position.

Comments:

Reference:

HP:0011126

Genes and Diseases:

Child Nodes:

Sister Nodes:

Ectopic kidney (HP:0000086)

Horseshoe kidney (HP:0000085)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011126	HP:0011126	Nephroptosis	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.