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Disease Ontology Browser
nemaline myopathy 1 (DOID:0110926)
Alliance: disease page
Synonyms: congenital myopathy 4B; NEM1; nemaline myopathy 1, autosomal dominant or recessive
Alt IDs: OMIM:609284, MESH:C538348
Definition: A nemaline myopathy characterized by onset typically in early childhood of mildly delayed motor development, hypotonia, generalized muscle weakness, and weakness of the proximal limb muscles and neck muscles, resulting in difficulty running and easy fatigability that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the TPM3 gene on chromosome 1q21.

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
MGI 6.13
The Jackson Laboratory