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Human Disease

familial gestational hyperthyroidism

Term ID
DOID:0081102
Synonyms
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. https://pubmed.ncbi.nlm.nih.gov/9267761/
References
Ontology
Human Disease   ( DOID:0081102 )
Relationships
is a type of
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Genes Involved
Zebrafish Models