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 macular morphology (HP:0001103)

Grandparent Node:
Abnormal morphology of the choroidal vasculature (HP:0025568)

Parent Node:
Choroidal neovascularization (HP:0011506)

..Starting node
..Subfoveal choroidal neovascularization (HP:0031241)

Term ID:

31241

Name:

Subfoveal choroidal neovascularization

Synonym:

Definition:

A type of choroidal neovascularization in which the area of neovascularization overlaps with the center of the fovea.

Comments:

Reference:

HP:0031241

Genes and Diseases:

Child Nodes:

Sister Nodes:

Extrafoveal choroidal neovascularization (HP:0031239)

Juxtafoveal choroidal neovascularization (HP:0031240)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031241	HP:0031241	Subfoveal choroidal neovascularization	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.