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Disease Ontology Browser
nemaline myopathy 7 (DOID:0110934)
Alliance: disease page
Synonyms: NEM7; nemaline myopathy 7, autosomal recessive
Alt IDs: OMIM:610687
Definition: A nemaline myopathy characterized by very early onset of hypotonia and delayed motor development that has_material_basis_in homozygous mutation in the CFL2 gene on chromosome 14q13.


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
02/18/2020
MGI 6.14
The Jackson Laboratory