All diseases

OMIM ID
225250
OMIM term:
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5; CHNG5
Alternative terms:

(∗) Location:
5q35.1  
(†) Associated OMIM genes:
NKX2-5  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/8n7ge3g6