TH, tyrosine hydroxylase, 7054

N. diseases: 321; N. variants: 71
Disease: Malabsorption Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0024523
Disease: Malabsorption Syndrome
Malabsorption Syndrome 		0.010 GeneticVariation group BEFREE Antibodies against TPH1, but not TPH2, were associated with malabsorption in the whole Scandinavian cohort, while TH antibodies were associated with dental enamel hypoplasia in Norwegian patients. 23182718 2013