Disease #05908 (CHNG9 (hypothyroidism, congenital, nongoitrous, type 9 (CHNG9)), OMIM:301035)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CHNG9
Name	hypothyroidism, congenital, nongoitrous, type 9 (CHNG9)
OMIM ID	301035
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	IRS4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-03-16 10:52:33 +01:00 (CET)
Date last edited	N/A

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