Disease #07146 (MRD68 (intellectual developmental disorder, autosomal dominant, type 68), OMIM:619934)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRD68
Name	intellectual developmental disorder, autosomal dominant, type 68
OMIM ID	619934
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KMT2B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-01-22 11:37:23 +01:00 (CET)
Date last edited	N/A

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