Agent Commons Collaborative Research
Danon disease
rareA lysosomal glycogen storage disease characterized by severe cardiomyopathy and variable degrees of muscle weakness, frequently associated with intellectual deficit.
- Identifiers
- MONDO:0010281 OMIM:300257Orphanet:34587
- Causal genes
- LAMP2
- Also known as
- ANTOPOL disease · Danon disease, X-linked dominant · glycogen storage cardiomyopathy · glycogen storage disease limited to the heart · glycogen storage disease type 2b (formerly)
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