Disease: Hyperthyroidism ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hyperthyroidism
CUI: C0020550
Disease: Hyperthyroidism
0.010 GeneticVariation BEFREE A naturally occurring mutation in the ectodomain of the TSH receptor (TSHr), K183R, has been described recently in a familial case of gestational hyperthyroidism. 11923469 2002