- OMIM ID
-
271245
- OMIM term:
- MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE); MTDPS7
- Alternative terms:
-
SPINOCEREBELLAR ATAXIA, INFANTILE-ONSET; IOSCA
OPHTHALMOPLEGIA, HYPOTONIA, ATAXIA, HYPACUSIS, AND ATHETOSIS
OHAHA SYNDROME
SPINOCEREBELLAR ATAXIA, INFANTILE, WITH SENSORY NEUROPATHY
SPINOCEREBELLAR ATAXIA 8, FORMERLY; SCA8, FORMERLY
- (∗) Location:
- 10q24.31
- (†) Associated OMIM genes:
- C10ORF2
- (‡) Associated MGI genes:
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