About   Help   FAQ
Disease Ontology Browser
autosomal dominant limb-girdle muscular dystrophy type 1G (DOID:0110306)
Alliance: disease page
Synonyms: LGMD1G; muscular dystrophy limb-girdle type 1G
Alt IDs: OMIM:609115, ICD10CM:G71.0, ORDO:55596
Definition: An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the HNRNPDL gene on chromosome 4q21.

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
MGI 6.13
The Jackson Laboratory