Disease #05267 (LGMD2W;MDRCMTT (dystrophy, muscular, autosomal recessive, with cardiomyopathy and triangular tongue (LGMD-2W)), OMIM:616827)

Official abbreviation	LGMD2W;MDRCMTT
Name	dystrophy, muscular, autosomal recessive, with cardiomyopathy and triangular tongue (LGMD-2W)
OMIM ID	616827
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LIMS2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2017-05-05 19:27:35 +02:00 (CEST)
Date last edited	2024-01-12 21:08:38 +01:00 (CET)

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Global Variome shared LOVD