TH, tyrosine hydroxylase, 7054

N. diseases: 321; N. variants: 71
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.040 Biomarker group BEFREE Because of its key regulatory role in central and peripheral catecholamine synthesis, TH is associated with the pathogenesis of several neurological and psychiatric diseases, including Parkinson's disease, dystonia, schizophrenia, affective disorders, and cardiovascular diseases. 23537934 2013
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.040 GeneticVariation group BEFREE Does common genetic variation at human TH alter autonomic activity and predispose to cardiovascular disease? 19120120 2008
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.040 GeneticVariation group BEFREE Does common genetic variation at human TH alter autonomic activity and predispose to cardiovascular disease? 17698732 2007
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.040 GeneticVariation group BEFREE We conclude that common allelic variation within the tyrosine hydroxylase locus exerts a powerful, heritable effect on autonomic control of the circulation and that such variation may have implications in later development of cardiovascular disease traits such as hypertension. 15367723 2004