Disease #01100 (MDDGC4;LGMDR13;LGMD2M (dystrophy-dystroglycanopathy, muscular, (limb-girdle), type 4 (LGMDR13, LGMD2M)), OMIM:611588)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MDDGC4;LGMDR13;LGMD2M
Name	dystrophy-dystroglycanopathy, muscular, (limb-girdle), type 4 (LGMDR13, LGMD2M)
OMIM ID	611588
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FKTN
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2024-01-12 21:46:51 +01:00 (CET)

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