nemaline myopathy 4 Disease Ontology Browser

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Disease Ontology Browser

nemaline myopathy 4 (DOID:0110932)
Alliance: disease page
Synonyms: CAP myopathy 2; NEM4; nemaline myopathy 4, autosomal dominant
Alt IDs: OMIM:609285, MESH:C538351
Definition: A nemaline myopathy that has_material_basis_in heterozygous mutation in the TPM2 gene on chromosome 9p13.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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