Disease #05836 (MRD51 (mental retardation, autosomal dominant, type 51 (MRD51)), OMIM:617788)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRD51
Name	mental retardation, autosomal dominant, type 51 (MRD51)
OMIM ID	617788
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SUV420H1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-09-24 16:37:39 +02:00 (CEST)
Date last edited	N/A

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