Disease #01766 (CHNG-5 (hypothyroidism, congenital, nongoitrous, type 5 (CHNG-5), OMIM:225250)

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Official abbreviation	CHNG-5
Name	hypothyroidism, congenital, nongoitrous, type 5 (CHNG-5
OMIM ID	225250
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NKX2-5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A