Disease #02350 (LGMDR6;LGMD2F (dystrophy, muscular, limb-girdle, autosomal recessive, type 6 (LGMD2F)), OMIM:601287)

Official abbreviation	LGMDR6;LGMD2F
Name	dystrophy, muscular, limb-girdle, autosomal recessive, type 6 (LGMD2F)
OMIM ID	601287
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SGCD
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2024-01-12 20:51:43 +01:00 (CET)

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Global Variome shared LOVD