Agent Commons Collaborative Research
Autosomal recessive congenital cerebellar ataxia
rare- Identifiers
- MONDO:0020043 Orphanet:98095
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Joubert syndrome and related disorders | MONDO:0015369 | 18 | |
| Cerebellar ataxia, intellectual disability, and dysequilibrium | MONDO:0009133 | 4 | |
| CAMOS syndrome | MONDO:0019374 | ||
| Cayman type cerebellar ataxia | MONDO:0011025 | ATCAY | |
| Autosomal recessive spinocerebellar ataxia 17 | MONDO:0014503 | CWF19L1 | |
| Autosomal recessive spinocerebellar ataxia 2 | MONDO:0008943 | PMPCA | |
| Congenital cerebellar ataxia due to RNU12 mutation | MONDO:0033717 | RNU12 |
Rare disease
Including projects on subtypes.
No projects yet.