Disease #06582 (MDDGC8;LGMDR24 (dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C8), OMIM:618135)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MDDGC8;LGMDR24
Name	dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C8
OMIM ID	618135
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	POMGNT2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	2024-01-12 21:19:55 +01:00 (CET)

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