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Disease Ontology Browser
nemaline myopathy 4 (DOID:0110932)
Alliance: disease page
Synonyms: NEM4; nemaline myopathy 4, autosomal dominant
Alt IDs: OMIM:609285
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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last database update
07/09/2019
MGI 6.14
The Jackson Laboratory