Human Phenotype Ontology 
Grandparent Node:
Melanoma (HP:0002861)help
Grandparent Node:
Neoplasm of the eye (HP:0100012)help
Parent Node:
Uveal melanoma (HP:0007716)help
..Starting node
Choroidal melanoma (HP:0012054)help
Term ID: 12054
Name: Choroidal melanoma
Definition: Malignant tumor of melanocytes of the choroid. The classic appearance of choroidal melanoma is a pigmented dome-shaped or collar button-shaped tumor with an associated exudative retinal detachment. Choroidal melanoma is usually pigmented, but can be variably pigmented and even amelanotic (non-pigmented).
Reference: HP:0012054
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandCiliary body melanoma (HP:0012055) help
..expandIris melanoma (HP:0011524) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HP:0012054HP:0012054Choroidal melanoma0BAP1 CL E G H831439044ORPHA11191261950603089
HP:0012054HP:0012054Choroidal melanoma0CYSLTR2 CL E G H5710539044ORPHA126218274605666
HP:0012054HP:0012054Choroidal melanoma0GNA11 CL E G H276739044ORPHA111624379139313
HP:0012054HP:0012054Choroidal melanoma0GNAQ CL E G H277639044ORPHA16584390600998
HP:0012054HP:0012054Choroidal melanoma0SF3B1 CL E G H2345139044ORPHA146410768605590
HPO disease - gene - phenotype less frequent non-typical associations:

Genes (5) :BAP1 CYSLTR2 GNA11 GNAQ SF3B1

Diseases (1) :39044

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.