eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | arthrogryposis multiplex congenita |
| Comorbidity | C0023264|leigh syndrome |
| Sentences | 1 |
| PubMedID- 26016410 | These findings suggest that gfm2 mutations could be causative of a phenotype of leigh syndrome with arthrogryposis multiplex congenita. |
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