/congenital myopathy 23

congenital myopathy 23

Rare Disease

MONDO:0012240

Also Known As

CAPM2NEM4TPM2 nemaline myopathycap myopathy 2nemaline myopathy 4nemaline myopathy 4, autosomal dominantnemaline myopathy caused by mutation in TPM2nemaline myopathy type 4

Definition

Any nemaline myopathy in which the cause of the disease is a mutation in the TPM2 gene.

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Comprehensive, easy-to-understand information about this condition

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Associated Genes

TPM2 ↗

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

External Resources

OMIM

OMIM:609285 ↗

GARD

GARD:15454 ↗

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