C2677589 |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9 |
DO |
primary coenzyme Q10 deficiency 4
|
0070241 |
C2677589 |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9 |
MONDO |
autosomal recessive ataxia due to ubiquinone deficiency
|
0012784 |
C2677589 |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9 |
MSH |
Spinocerebellar Ataxia, Autosomal Recessive 9
|
C567436 |
C2677589 |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9 |
OMIM |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9
|
612016 |
C2677589 |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9 |
OMIM |
COENZYME Q10 DEFICIENCY, PRIMARY, 4
|
612016 |
C2677589 |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9 |
ORDO |
Autosomal recessive ataxia due to ubiquinone deficiency
|
139485 |