All diseases

OMIM ID
274600
OMIM term:
PENDRED SYNDROME; PDS
Alternative terms:
DEAFNESS WITH GOITER
GOITER-DEAFNESS SYNDROME
THYROID DYSHORMONOGENESIS 2B; TDH2B
THYROID HORMONOGENESIS, GENETIC DEFECT IN, 2B
HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 2B
(∗) Location:
7q22.3  
(†) Associated OMIM genes:
SLC26A4  
(‡) Associated MGI genes:
Foxi1   Slc26a4  

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