myopathy, centronuclear, 2

Rare Disease

MONDO:0009709

Also Known As

BIN1 centronuclear myopathycentronuclear myopathy 2centronuclear myopathy caused by mutation in BIN1myopathy, centronuclear, 2myopathy, centronuclear, type 2CNM2myopathy, centronuclear, autosomal recessivemyotubular myopathy, autosomal recessive

Definition

Any centronuclear myopathy in which the cause of the disease is a mutation in the BIN1 gene.

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Associated Genes

BIN1 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:255200 ↗

GARD

GARD:15208 ↗

Related Diseases

myopathy, centronuclear, 5

MONDO:0014418

Rare

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