| 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
|
- |
- |