About   Help   FAQ
Disease Ontology Browser
distal myopathy 1 (DOID:0070197)
Alliance: disease page
Synonyms: Distal myopathy type 1; Gowers disease; Laing distal myopathy; Laing early-onset distal myopathy; MPD1
Alt IDs: OMIM:160500, ORDO:59135
Definition: A distal myopathy that is characterized by autosomal dominant inheritance that has_material_basis_in mutation in the MYH7 gene on chromosome 14q11.2.


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, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory