- OMIM ID
-
213200
- OMIM term:
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2
- Alternative terms:
-
CEREBELLAR HYPOPLASIA, NONPROGRESSIVE NORMAN TYPE
CEREBELLAR GRANULAR CELL HYPOPLASIA AND MENTAL RETARDATION, CONGENITAL
CEREBELLOPARENCHYMAL DISORDER III
CPD III; CPD3
- (∗) Location:
- 9q34-qter
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
Loading mouse genes ...