Disease #03905 (LGMD-2T;MDDGC-14 (dystrophy, muscular, limb-girdle, type 2T (LGMD-2T, dystroglycanopathy C14 (MDDGC-14))), OMIM:615352)

Official abbreviation LGMD-2T;MDDGC-14
Name dystrophy, muscular, limb-girdle, type 2T (LGMD-2T, dystroglycanopathy C14 (MDDGC-14))
OMIM ID 615352
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GMPPB
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A