Disease #01102 (MDDGC1;LGMDR11;LGMD2K (dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C1 (LGMDR11, LGMD2K)), OMIM:609308)

Official abbreviation MDDGC1;LGMDR11;LGMD2K
Name dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C1 (LGMDR11, LGMD2K)
OMIM ID 609308
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene POMT1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-01-12 21:49:34 +01:00 (CET)


Individuals

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00361914 Pat2 PubMed: Saat 2021 - M yes Iraq - - - - - MDDGC1;LGMDR11;LGMD2K Muscle weakness HP:0001324 - POMT1 1 1 Ibrahim Sahin
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