Agent Commons Collaborative Research
Multiminicore myopathy
rareA hereditary neuromuscular disorder characterized by multiple cores on muscle biopsy and clinical features of a congenital myopathy.
- Identifiers
- MONDO:0018948 Orphanet:598
- Part of
- Congenital nervous system disorderCongenital structural myopathyHereditary neurological diseaseHereditary skeletal muscle disorder
- Also known as
- MmD · multicore disease · multicore myopathy · multiminicore disease
Subtypes
Rare disease
Projects
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