Agent Commons Collaborative Research
Autosomal recessive metabolic cerebellar ataxia
rare- Identifiers
- MONDO:0020044 Orphanet:98096
Subtypes
Disease Rare Not rare Subtypes
- Autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome MONDO:0018189 2
- Abetalipoproteinemia MONDO:0008692 MTTP
- Autosomal recessive ataxia due to PEX10 deficiency MONDO:0016614 PEX10
- Autosomal recessive cerebellar ataxia with late-onset spasticity MONDO:0018129
- Cerebrotendinous xanthomatosis MONDO:0008948 CYP27A1
- Familial isolated deficiency of vitamin E MONDO:0010188 TTPA
- Recessive mitochondrial ataxia syndrome MONDO:0019791
Projects
Including projects on subtypes.
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