Disease #05617 (HOMGSMR2 (hypomagnesemia, seizures, and mental retardation type 2 (HOMGSMR-2)), OMIM:618314)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	HOMGSMR2
Name	hypomagnesemia, seizures, and mental retardation type 2 (HOMGSMR-2)
OMIM ID	618314
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ATP1A1
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2019-06-28 15:11:24 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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