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:
Embryonal renal neoplasm (HP:0011794)

Parent Node:
Nephroblastomatosis (HP:0008643)

..Starting node
..Intralobar nephroblastomatosis (HP:0011795)

Term ID:

11795

Name:

Intralobar nephroblastomatosis

Synonym:

Definition:

Presence of persistent islands of renal blastema in the postnatal kidney, anywhere within a renal lobe (a portion of a kidney consisting of a renal pyramid and the renal cortex above it).

Comments:

Reference:

HP:0011795

Genes and Diseases:

Child Nodes:

Sister Nodes:

Perilobar nephroblastomatosis (HP:0011796)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011795	HP:0011795	Intralobar 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.

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