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Disease Ontology Browser
nemaline myopathy 11 (DOID:0110933)
Alliance: disease page
Synonyms: NEM11; nemaline myopathy 11, autosomal recessive
Alt IDs: OMIM:617336
Definition: A nemaline myopathy characterized by onset of slowly progressive muscle weakness in the first decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the MYPN gene on chromosome 10q21.

Disease References using Mouse Models (1)

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
01/31/2023
MGI 6.22
The Jackson Laboratory