Disease #00169 (CMM2 (MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2), OMIM:155601)

Official abbreviation CMM2
Name MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
OMIM ID 155601
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CDKN2A
Associated tissues -
Disease features -
Remarks -

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