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 glomerulus morphology (HP:0000095)

Grandparent Node:
Nephritis (HP:0000123)

Parent Node:
Glomerulonephritis (HP:0000099)

..Starting node
..Crescentic glomerulonephritis (HP:0008653)

Term ID:

8653

Name:

Crescentic glomerulonephritis

Synonym:

Definition:

A type of extracapillary glomerulonephritis characterized by the formation of crescent-like cellular proliferation.

Comments:

Reference:

HP:0008653

Genes and Diseases:

Child Nodes:

Sister Nodes:

Membranoproliferative glomerulonephritis (HP:0000793)

Membranous nephropathy (HP:0012578)

Minimal change glomerulonephritis (HP:0012579)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008653	HP:0008653	Crescentic glomerulonephritis	0	COPA CL E G H	1314	2230	OMIM:616414	AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE; AILJK	5

Genes (1) :COPA

Diseases (1) :OMIM:616414

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.