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:
Embryonal renal neoplasm (HP:0011794)

Parent Node:
Nephroblastomatosis (HP:0008643)

..Starting node
..Perilobar nephroblastomatosis (HP:0011796)

Term ID:

11796

Name:

Perilobar nephroblastomatosis

Synonym:

Definition:

Abnormally persistent foci of embryonal immature blastema located in the superficial cortical region (perilobar).

Comments:

Reference:

HP:0011796

Genes and Diseases:

Child Nodes:

Sister Nodes:

Intralobar nephroblastomatosis (HP:0011795)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011796	HP:0011796	Perilobar nephroblastomatosis	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.