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Disease Ontology Browser
nemaline myopathy 2 (DOID:0110928)
Alliance: disease page
Synonyms: NEM2; nemaline myopathy 2, autosomal recessive
Alt IDs: OMIM:256030
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 (4)

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
02/04/2020
MGI 6.14
The Jackson Laboratory