About   Help   FAQ
Disease Ontology Browser
nemaline myopathy 4 (DOID:0110932)
Alliance: disease page
Synonyms: NEM4; nemaline myopathy 4, autosomal dominant
Alt IDs: OMIM:609285
Definition: A nemaline myopathy that has_material_basis_in heterozygous mutation in the TPM2 gene on chromosome 9p13.

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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.14
The Jackson Laboratory