Disease #00430 (MFM1;LGMD2R (yopathy, myofibrillar,, type 1 (LGMD2R)), OMIM:615325)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MFM1;LGMD2R
Name	yopathy, myofibrillar,, type 1 (LGMD2R)
OMIM ID	615325
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DES
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-06-20 20:44:58 +02:00 (CEST)
Date last edited	2024-01-12 21:06:51 +01:00 (CET)

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