- OMIM ID
-
108500
- OMIM term:
- EPISODIC ATAXIA, TYPE 2; EA2
- Alternative terms:
-
ATAXIA, EPISODIC, WITH NYSTAGMUS
EPISODIC ATAXIA, NYSTAGMUS-ASSOCIATED
CEREBELLOPATHY, HEREDITARY PAROXYSMAL
ATAXIA, FAMILIAL PAROXYSMAL
ACETAZOLAMIDE-RESPONSIVE HEREDITARY PAROXYSMAL CEREBELLAR ATAXIA; APCA
CEREBELLAR ATAXIA, PAROXYSMAL, ACETAZOLAMIDE-RESPONSIVE; CAPA
- (∗) Location:
- 19p13.2
- (†) Associated OMIM genes:
- CACNA1A
- (‡) Associated MGI genes:
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