Disease #00818 (MRD-10 (mental retardation, autosomal dominant, type 10 (MRD-10)), OMIM:614256)

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	Curator: Johan T. den Dunnen

Official abbreviation	MRD-10
Name	mental retardation, autosomal dominant, type 10 (MRD-10)
OMIM ID	614256
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CACNG2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A