- OMIM ID
-
274400
- OMIM term:
- THYROID DYSHORMONOGENESIS 1; TDH1
- Alternative terms:
-
THYROID HORMONOGENESIS, GENETIC DEFECT IN, 1
HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 1
IODINE ACCUMULATION, TRANSPORT, OR TRAPPING DEFECT
- (∗) Location:
- 19p13.11
- (†) Associated OMIM genes:
- SLC5A5
- (‡) Associated MGI genes:
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