- OMIM ID
-
183090
- OMIM term:
- SPINOCEREBELLAR ATAXIA 2; SCA2
- Alternative terms:
-
SPINOCEREBELLAR ATROPHY II
OLIVOPONTOCEREBELLAR ATROPHY, HOLGUIN TYPE
OLIVOPONTOCEREBELLAR ATROPHY II; OPCA2
SPINOCEREBELLAR ATAXIA, CUBAN TYPE
CEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS
WADIA-SWAMI SYNDROME
SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS; SDSEM AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13, INCLUDED; ALS13, INCLUDED
- (∗) Location:
- 12q24.12
- (†) Associated OMIM genes:
- ATXN2
- (‡) Associated MGI genes:
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