All diseases

OMIM ID
609152
OMIM term:
HYPERTHYROIDISM, NONAUTOIMMUNE
Alternative terms:
HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE
HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT
TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT
(∗) Location:
14q31.1  
(†) Associated OMIM genes:
TSHR  
(‡) Associated MGI genes:

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