Phenotype #0000281482

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	00387913
Associated disease	CHNG5
Phenotype details	Congenital hypothyroidism (HP:0000851)
Diagnosis/Initial	-
Inheritance	Unknown
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Alaaeldin Fayez
Database submission license
Created by	Alaaeldin Fayez
Date created	2021-10-31 15:05:33 +01:00 (CET)
Date last edited	2022-04-07 12:24:41 +02:00 (CEST)

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