LCT, lactase, 3938

N. diseases: 90; N. variants: 14
Disease: AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2751492
Disease: AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED 		0.010 GeneticVariation disease BEFREE The C/C genotype of the lactase gene was observed in 39.1% subjects with no significant difference between UC and FAP patients. 31137035 2019