Disease: Thyrotoxicosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Thyrotoxicosis
CUI: C0040156
Disease: Thyrotoxicosis
0.010 GeneticVariation BEFREE Long-term follow-Up of an infant with thyrotoxicosis due to germline mutation of the TSH receptor gene (Met453Thr). 10095169 1999