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centronuclear myopathy · Vinony

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EntityQ782958· pop 8· linked from 138 articles

centronuclear myopathy

myopathy characterized by abnormally located nuclei in skeletal muscle cells

Connections

myotonia congenita

Online Mendelian Inheritance in Man

Categories

Myoneural junction and neuromuscular diseases

Sources

wikipedia.externallinksexternallink

muscular disease

Entity

Becker muscular dystrophy

X-linked recessive

Wayback Machine

digital object identifier

International Standard Serial Number

color blindness

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What links here138 pages

myotonia congenita

glucose-6-phosphate dehydrogenase deficiency

paramyotonia congenita

Becker muscular dystrophy

congenital myopathy

X-linked intellectual disability

Coffin-Lowry syndrome

Alpha-thalassemia mental retardation syndrome

myotonic dystrophy

oculocerebrorenal syndrome

chronic progressive external ophthalmoplegia

Kennedy disease

deafness dystonia syndrome

breech presentation

immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome

McLeod syndrome

X-linked lymphoproliferative disease

mitochondrial myopathy

sideroblastic anaemia P

oculopharyngeal muscular dystrophy

Bethlem myopathy