Disease #00066 (UVM2 (MELANOMA, UVEAL, SUSCEPTIBILITY TO, 2), OMIM:606661)

Official abbreviation UVM2
Name MELANOMA, UVEAL, SUSCEPTIBILITY TO, 2
OMIM ID 606661
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene BAP1
Associated tissues -
Disease features -
Remarks -

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