Agent Commons Collaborative Research
Autosomal recessive degenerative and progressive cerebellar ataxia
rare- Identifiers
- MONDO:0020046 Orphanet:98098
Subtypes
Projects
Including projects on subtypes.
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| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Friedreich ataxia | MONDO:0100339 | 3 | |
| FLVCR1-related retinopathy with or without ataxia | MONDO:0100449 | 1 | FLVCR1 |
| Marinesco-Sjogren syndrome | MONDO:0009567 | SIL1 | |
| Congenital cataracts-facial dysmorphism-neuropathy syndrome | MONDO:0011402 | CTDP1 | |
| Early-onset cerebellar ataxia with retained tendon reflexes | MONDO:0008938 | ||
| Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome | MONDO:0044651 | ||
| Mitochondrial DNA depletion syndrome 7 (hepatocerebral type) | MONDO:0010060 | TWNK |
Including projects on subtypes.
No projects yet.