Disease #05906 (CHNG7 (hypothyroidism, congenital, nongoitrous, type 7 (CHNG7)), OMIM:618573)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CHNG7
Name	hypothyroidism, congenital, nongoitrous, type 7 (CHNG7)
OMIM ID	618573
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TRHR
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-03-16 10:48:35 +01:00 (CET)
Date last edited	N/A

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