Disease #07173 (MRD66 (intellectual developmental disorder, autosomal dominant, type 66), OMIM:619910)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MRD66
Name	intellectual developmental disorder, autosomal dominant, type 66
OMIM ID	619910
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ATP2B1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-08-29 19:38:30 +02:00 (CEST)
Date last edited	N/A

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