Disease #01441 (MRMV-1 (mirror movements, type 1 (MRMV-1, congenital)), OMIM:157600)

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Official abbreviation	MRMV-1
Name	mirror movements, type 1 (MRMV-1, congenital)
OMIM ID	157600
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DCC
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A