- OMIM ID
-
275100
- OMIM term:
- HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4; CHNG4
- Alternative terms:
-
THYROTROPIN DEFICIENCY, ISOLATED
THYROID-STIMULATING HORMONE DEFICIENCY
TSH DEFICIENCY
PITUITARY CRETINISM THYROTROPIN, BIOLOGICALLY INACTIVE, INCLUDED
- (∗) Location:
- 1p13.2
- (†) Associated OMIM genes:
- TSHB
- (‡) Associated MGI genes:
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