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Disease Ontology Browser
nemaline myopathy 2 (DOID:0110928)
Alliance: disease page
Synonyms: congenital myopathy 2; NEM2; nemaline myopathy 2, autosomal recessive
Alt IDs: OMIM:256030, MESH:C538349
Definition: A nemaline myopathy that has_material_basis_in homozygous or compound heterozygous mutation in the NEB gene on chromosome 2q23.

Disease References using Mouse Models (6)
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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory