Disease #03445 (MDDGC9;LGMDR16;LGMD2P (dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C9 (LGMDR16, LGMD2P)), OMIM:613818)

Official abbreviation MDDGC9;LGMDR16;LGMD2P
Name dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C9 (LGMDR16, LGMD2P)
OMIM ID 613818
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene DAG1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-01-12 21:36:55 +01:00 (CET)

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