Human Phenotype Ontology 
Grandparent Node:
Abnormal choroid morphology (HP:0000610)help
Parent Node:
Abnormal morphology of the choroidal vasculature (HP:0025568)help
..Starting node
Polypoidal choroidal vasculopathy (HP:0025569)help
Term ID: 25569
Name: Polypoidal choroidal vasculopathy
Definition: The presence of aneurysmal polypoidal lesions in the choroidal vasculature. The aneurysmal dilatations, also known as polyps, may be found at subfoveal, juxtafoveal, extrafoveal, peripapillary or even peripheral regions. These polypoidal dilatations may be visible as reddish-orange subretinal nodules during ophthalmoscopic examination. The polypoidal lesions are best detected on indocyanine green angiography (ICGA) and might be associated with a branching vascular network (BVN) of neovascularization.
Reference: HP:0025569
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandChoroidal hemangioma (HP:0007872) help
..expandChoroidal neovascularization (HP:0011506) help
..expandChoroidal vascular hyperpermeability (HP:0025570) help
..expandDilatation of large choroidal vessels (HP:0030979) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025569HP:0025569Polypoidal choroidal vasculopathy0 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 June 2019 release.