PedAM
Pediatric Disease Annotations & Medicines
| Disease | neutropenia |
| Phenotype | C0162670|mitochondrial myopathy |
| Sentences | 1 |
| PubMedID- 23045169 | Barth syndrome (bths); mim accession # 302060) is a rare x-linked recessive cardioskeletal mitochondrial myopathy with features of cardiomyopathy, neutropenia, and growth abnormalities. |
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