familial gestational hyperthyroidism (DOID:0081102)
Alliance: disease page
Alt IDs: OMIM:603373, ORDO:99819
Definition: A hyperthyroidism that is characterized by promiscuous stimulation of the thyrotropin receptor by the excess chorionic gonadotropin and that has_material_basis_in heterozygous mutation in the gene encoding the thyroid-stimulating hormone receptor (TSHR) on chromosome 14q31.