All diseases

OMIM ID
274900
OMIM term:
THYROID DYSHORMONOGENESIS 5; TDH5
Alternative terms:
THYROID HORMONOGENESIS, GENETIC DEFECT IN, 5
HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 5
(∗) Location:
15q21.1  
(†) Associated OMIM genes:
DUOXA2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/3ont7ysa