All diseases

OMIM ID
274800
OMIM term:
THYROID DYSHORMONOGENESIS 4; TDH4
Alternative terms:
THYROID HORMONOGENESIS, GENETIC DEFECT IN, 4
HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 4
IODOTYROSINE DEHALOGENASE DEFICIENCY
DEIODINASE DEFICIENCY
(∗) Location:
6q25.1  
(†) Associated OMIM genes:
IYD  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/5ed9wk6j