autosomal recessive metabolic cerebellar ataxia
MONDO:0020044Mondo
Findings
No curated finding names autosomal recessive metabolic cerebellar ataxia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Where it sits
- Narrower terms (7)
- abetalipoproteinemia
- autosomal recessive ataxia due to PEX10 deficiency
- autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome
- autosomal recessive cerebellar ataxia with late-onset spasticity
- cerebrotendinous xanthomatosis
- familial isolated deficiency of vitamin E
- recessive mitochondrial ataxia syndrome