Disease #00810 (MRD-13 (mental retardation, autosomal dominant, type 13 (MRD-13)), OMIM:614563)

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Official abbreviation	MRD-13
Name	mental retardation, autosomal dominant, type 13 (MRD-13)
OMIM ID	614563
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DYNC1H1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A