Phenotype #0000306091

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00414236
Associated disease	HOMG1
Phenotype details	Hypomagnesemia, Seizure
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Andreas Laner
Database submission license
Created by	Andreas Laner
Date created	2022-07-28 10:14:09 +02:00 (CEST)
Date last edited	2022-07-29 10:07:45 +02:00 (CEST)

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