Disease #01343 (CMNS (nevus syndrome, melanocytic, congenital, somatic), OMIM:137550)

Official abbreviation CMNS
Name nevus syndrome, melanocytic, congenital, somatic
OMIM ID 137550
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes HRAS, NRAS
Associated tissues -
Disease features -
Remarks -