Human Phenotype Ontology 
Grandparent Node:
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Melanoma (HP:0002861)help
Grandparent Node:
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Neoplasm of the eye (HP:0100012)help
Parent Node:
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Abnormal ciliary body morphology (HP:0012776)help
Parent Node:
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Uveal melanoma (HP:0007716)help
..Starting node
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Ciliary body melanoma (HP:0012055)help
Term ID: 12055
Name: Ciliary body melanoma
Synonym:
Definition: Malignant tumor of melanocytes of the ciliary body.
Comments:
Reference: HP:0012055
Genes and Diseases:
 
       Child Nodes:

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