Phenotype #0000173792

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00231400
Associated disease	HOMG1
Phenotype details	hypomagnesemia (HP:0002917), hypocalcaemia (HP:0002901)
Diagnosis/Initial	HSH
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	HSH
Age/Examination	05y (5 years)
Age/Diagnosis	05y
Age/Onset	00y01m
Phenotype/Onset	-
Protein	-
Owner name	John Sayer
Database submission license
Created by	John Sayer
Date created	2019-05-01 16:02:48 +02:00 (CEST)
Date last edited	2019-05-02 08:17:45 +02:00 (CEST)

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