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: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
0.020 GeneticVariation disease BEFREE The TH-encoding gene contains a tetrameric short tandem repeat in intron 1 (TH01), with allele 9.3 reported to be associated with SIDS in German infants. 24975687 2014
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
0.020 GeneticVariation disease LHGDN A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome. 18534229 2008
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
0.020 GeneticVariation disease BEFREE A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome. 18534229 2008