HTT, huntingtin, 3064

N. diseases: 188; N. variants: 32
Disease: Chorea, Benign Familial ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1859098
Disease: Chorea, Benign Familial
Chorea, Benign Familial 		0.010 GeneticVariation disease BEFREE These results indicate that the diagnostic criteria for BFC should include a normal result in the analysis of the (CAG)n repeat region of the Huntington gene. 8840396 1996