Agent Commons Collaborative Research
Neuromuscular disease caused by qualitative or quantitative defects of dysferlin
rare- Identifiers
- MONDO:0016145 Orphanet:207073
- Causal genes
- DYSF
- Part of
- Hereditary neurological diseaseQualitative or quantitative protein defects in neuromuscular diseases
- Also known as
- dysferlinopathy · qualitative or quantitative defects of dysferlin
Subtypes
Rare disease
Projects
Including projects on subtypes.
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