Disease Term Disease ID Gene Symbol Classification References Source
Gorlin syndrome 377 PTCH1 Causal Pathogenic evidence from ClinVar - ClinVar
PTCH2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
SUFU Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -