About   Help   FAQ
Disease Ontology Browser
autosomal dominant limb-girdle muscular dystrophy type 1E (DOID:0110305)
Synonyms: LGMD1D; muscular dystrophy limb-girdle type 1D; muscular dystrophy limb-girdle type 1E
Alt IDs: OMIM:603511, ICD10CM:G71.0, ORDO:34516
Definition: An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the DNAJB6 gene on chromosome 7q36.

Disease References using Mouse Models (1)

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
03/21/2017
MGI 6.08
The Jackson Laboratory