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autosomal dominant limb-girdle muscular dystrophy type 1G (DOID:0110306)
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
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last database update
05/16/2017
MGI 6.09
The Jackson Laboratory