Disease #04303 (MRMV3 (mirror movements, type 3 (MRMV-3)), OMIM:616059)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	MRMV3
Name	mirror movements, type 3 (MRMV-3)
OMIM ID	616059
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DNAL4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-07-19 11:48:48 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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