Disease Term Disease ID Gene Symbol Classification References Source
Huntington disease-like 1 157941 PRNP Causal Pathogenic evidence from ClinVar - ClinVar
HUNTINGTON DISEASE-LIKE 1 C1864112 PRNP Causal Pathogenic evidence from ClinVar 1363809, 1363810, 2572450, 8939199, 9813003, 10079068, 10360778, 11593450, 11756597, 11839833, 12372829, 14967768, 15366237, 16831973, 16939293, 17494694, 20139714, 20514992, 20541558, 20593190, 21298055, 22072968, 22318125, 22584955, 23132868, 23296137, 23723004, 24275071, 25064618, 25522698, 25959220, 26791950, 27803826 ClinVar
Huntington disease-like syndrome due to C9ORF72 expansions 401901 C9orf72 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
Huntington disease-like 2 98934 JPH3 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
HUNTINGTON DISEASE-LIKE 2 C1847987 JPH3 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
Huntington Disease-Like Syndrome C3711380 PSEN2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -