Disease #04655 (MRD-29 (mental retardation, autosomal dominant, type 29 (MRD-29)), OMIM:616078)

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	Curator: Johan T. den Dunnen

Official abbreviation	MRD-29
Name	mental retardation, autosomal dominant, type 29 (MRD-29)
OMIM ID	616078
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SETBP1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:23 +02:00 (CEST)
Date last edited	N/A