All diseases

OMIM ID
607200
OMIM term:
THYROID DYSHORMONOGENESIS 6; TDH6
Alternative terms:
THYROID HORMONOGENESIS, GENETIC DEFECT IN, 6
HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 6
(∗) Location:
15q21.1  
(†) Associated OMIM genes:
DUOX2  
(‡) Associated MGI genes:
Duox2  

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