Human Phenotype Ontology 
Grandparent Node:
Abnormal fundus morphology (HP:0001098)help
Grandparent Node:
Abnormal uvea morphology (HP:0000553)help
Parent Node:
Abnormal choroid morphology (HP:0000610)help
..Starting node
Choroidal nevus (HP:0025314)help
Term ID: 25314
Name: Choroidal nevus
Definition: A benign, flat or slightly elevated melanocytic lesions of the posterior uveawith clearly defined margins. Choroidal nevi tend they remain stable in size, and to display features such as overlying drusen as well as retinal pigment epithelial atrophy, hyperplasia or fibrous metaplasia.
Reference: HP:0025314
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAbnormal chorioretinal morphology (HP:0000532) help
..expandAbnormal morphology of the choroidal vasculature (HP:0025568) help
..expandBirdshot choroidal lesions (HP:0030952) help
..expandChoroideremia (HP:0001139) help
..expandDark choroid (HP:0025148) 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:0025314HP:0025314Choroidal nevus0 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.