Disease #05813 (MRD52 (mental retardation, autosomal dominant, type 52 (MRD52)), OMIM:617796)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRD52
Name	mental retardation, autosomal dominant, type 52 (MRD52)
OMIM ID	617796
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ASH1L
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-08-17 20:47:15 +02:00 (CEST)
Date last edited	N/A

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