Preferred Label : Genetic Predisposition to Melanoma;
NCIt definition : An inherited condition caused by mutation(s) in the CDKN2A or CDK4 genes, encoding
cyclin-dependent kinase inhibitor 2A and cyclin-dependent kinase 4, respectively.
The condition is characterized by an increased risk of developing melanoma.;
NCI Metathesaurus CUI : CL1662291;
Origin ID : C179472;
UMLS CUI : C5555718;
Semantic type(s)
concept_is_in_subset
related_to_genetic_biomarker