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

..Starting node
..Glomerular endocapillary leukocyte hypercellularity (HP:0033488)

Term ID:

33488

Name:

Glomerular endocapillary leukocyte hypercellularity

Synonym:

Glomerular endocapillary hypercellularity consisting of leukocytes

Definition:

Increased number of leukocytes internal to the glomerular basement membrane (GBM), but not limited to within glomerular capillaries.

Comments:

Reference:

HP:0033488

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0033488	HP:0033488	Glomerular endocapillary leukocyte hypercellularity	0	CL E G H
HP:0033488	HP:0033490	Glomerular endocapillary foam-cell hypercellularity	1	CL E G H
HP:0033488	HP:0033489	Glomerular endocapillary neutrophil hypercellularity	1	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.