Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4157
Gene Symbol: MC1R
MC1R
CUI: C2314896
Disease: Familial Atypical Mole Melanoma Syndrome
Familial Atypical Mole Melanoma Syndrome 		0.310 SusceptibilityMutation ORPHANET Clinical characteristics of patients with cutaneous melanoma according to variants in the melanocortin 1 receptor gene. 24238329

2014
Entrez Id: 4157
Gene Symbol: MC1R
MC1R
CUI: C2314896
Disease: Familial Atypical Mole Melanoma Syndrome
Familial Atypical Mole Melanoma Syndrome 		0.310 SusceptibilityMutation ORPHANET Melanoma susceptibility genes and risk assessment. 24258989

2014