Disease #05777 (LGMDR21;LGMD2Z (dystrophy, muscular, limb-girdle, recessive, type 21 (LGMDR21, LGMD2Z)), OMIM:617232)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	LGMDR21;LGMD2Z
Name	dystrophy, muscular, limb-girdle, recessive, type 21 (LGMDR21, LGMD2Z)
OMIM ID	617232
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	POGLUT1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-06-29 18:32:52 +02:00 (CEST)
Date last edited	N/A

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