Disease #00939 (LGMDR8;LGMD2H (dystrophy, muscular, limb-girdle, autosomal recessive, type 8 (LGMD2H)), OMIM:254110)

Official abbreviation	LGMDR8;LGMD2H
Name	dystrophy, muscular, limb-girdle, autosomal recessive, type 8 (LGMD2H)
OMIM ID	254110
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TRIM32
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2024-01-12 20:52:24 +01:00 (CET)

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Global Variome shared LOVD