FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term familial gestational hyperthyroidism ID (Ontology) DOID:0081102 (Human Disease)
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.
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 Genes
 familial gestational hyperthyroidism       1
 for disease ribbon | familial gestational hyperthyroidism       1
 model of | familial gestational hyperthyroidism       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
thyroid gland disease           |
 |__hyperthyroidism_____________|
                                familial gestational hyperthyroidism  1 rec.
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Is a autosomal dominant disease
hyperthyroidism
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MIM:603373
ORDO:99819