About   Help   FAQ
Disease Ontology Browser
autosomal dominant limb-girdle muscular dystrophy type 1F (DOID:0110304)
Alliance: disease page
Synonyms: LGMD1F; muscular dystrophy limb-girdle type 1F
Alt IDs: OMIM:608423, ICD10CM:G71.0, ORDO:55595
Definition: An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the TNPO3 gene on chromosome 7q32.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
12/05/2017
MGI 6.11
The Jackson Laboratory