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

MVZ für Humangenetik Regensburg

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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	-
Date created	2023-06-16 08:40:20 +00:00 (UTC)
Date last edited	N/A