Disease #03651 (CHNG6 (hypothyroidism, congenital, nongoitrous, type 6 (CHNG6)), OMIM:614450)

Global Variome shared LOVD

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Official abbreviation	CHNG6
Name	hypothyroidism, congenital, nongoitrous, type 6 (CHNG6)
OMIM ID	614450
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	THRA
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-03-16 10:46:22 +01:00 (CET)

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