- OMIM ID
-
274500
- OMIM term:
- THYROID DYSHORMONOGENESIS 2A; TDH2A
- Alternative terms:
-
THYROID HORMONOGENESIS, GENETIC DEFECT IN, 2A
HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 2A
IODIDE PEROXIDASE DEFICIENCY
THYROID PEROXIDASE DEFICIENCY
- (∗) Location:
- 2p25.3
- (†) Associated OMIM genes:
- TPO
- (‡) Associated MGI genes:
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