Disease: Hyperthyroidism, Nonautoimmune ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hyperthyroidism, Nonautoimmune
CUI: C1836706
Disease: Hyperthyroidism, Nonautoimmune
0.710 GeneticVariation BEFREE Identification of a new thyrotropin receptor germline mutation (Leu629Phe) in a family with neonatal onset of autosomal dominant nonautoimmune hyperthyroidism. 9398746 1997
Hyperthyroidism, Nonautoimmune
CUI: C1836706
Disease: Hyperthyroidism, Nonautoimmune
0.710 CausalMutation CLINVAR