All diseases

OMIM ID
275200
OMIM term:
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1; CHNG1
Alternative terms:
THYROTROPIN RESISTANCE
THYROID-STIMULATING HORMONE, RESISTANCE TO; RTSH
TSH RESISTANCE
HYPOTHYROIDISM, NONAUTOIMMUNE
HYPOTHYROIDISM, CONGENITAL, DUE TO TSH RESISTANCE
HYPOTHYROIDISM DUE TO UNRESPONSIVENESS TO THYROTROPIN
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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