Disease #01088 (MDDGC3;LGMDR15;LGMD2O (dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C3 (LGMDR15, LGMD2O)), OMIM:613157)

Official abbreviation MDDGC3;LGMDR15;LGMD2O
Name dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C3 (LGMDR15, LGMD2O)
OMIM ID 613157
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene POMGNT1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-01-12 21:40:00 +01:00 (CET)

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