All diseases

OMIM ID
274700
OMIM term:
THYROID DYSHORMONOGENESIS 3; TDH3
Alternative terms:
THYROID HORMONOGENESIS, GENETIC DEFECT IN, 3
HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 3
(∗) Location:
8q24.22  
(†) Associated OMIM genes:
TG  
(‡) Associated MGI genes:
Tg  

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