Multiminicore myopathy
MONDO:0018948A hereditary neuromuscular disorder characterized by multiple cores on muscle biopsy and clinical features of a congenital myopathy.
Also known as: MmD, multicore disease, multicore myopathy, multiminicore disease
1 clinical trial for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Rigid spine muscular dystrophy 1
(1)
Antenatal multiminicore disease with arthrogryposis multiplex congenita
(0)
Classic multiminicore myopathy
(0)
Congenital multicore myopathy with external ophthalmoplegia
(0)
Desmin-related myopathy with Mallory body-like inclusions
(0)
Moderate multiminicore disease with hand involvement
(0)
Broader categories
Disease
(679)
Nervous system disorder
(231)
Hereditary disease
(176)
Human disease
(14)
Hereditary neurological disease
(6)
Disease of genetic or genomic mechanism
(2)
Disease by body system or component
(0)
Disease by etiologic mechanism
(0)
Neuromuscular disease caused by qualitative or quantitative defects of selenoprotein N1
(0)
Qualitative or quantitative protein defects in neuromuscular diseases
(0)