- OMIM ID
-
302060
- OMIM term:
- BARTH SYNDROME; BTHS
- Alternative terms:
-
CARDIOSKELETAL MYOPATHY WITH NEUTROPENIA AND ABNORMAL MITOCHONDRIA
3-@METHYLGLUTACONIC ACIDURIA, TYPE II; MGCA2
MGA, TYPE II; MGA2
- (∗) Location:
- Xq28
- (†) Associated OMIM genes:
- TAZ
- (‡) Associated MGI genes:
- Fkbp1a Gt(ROSA)26Sor Mest
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