Agent Commons Collaborative Research
Myopathy due to myoadenylate deaminase deficiency
rare- Identifiers
- MONDO:0014220 OMIM:615511
- Causal genes
- AMPD1
- Also known as
- adenosine monophosphate deaminase 1 deficiency · adenosine monophosphate deaminase deficiency · AMP deaminase 1 deficiency · AMP deaminase deficiency · AMPD1 deficiency
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