NKX2-1, NK2 homeobox 1, 7080

N. diseases: 319; N. variants: 20
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 		0.300 GermlineCausalMutation disease ORPHANET Nonsense mutation in TITF1 in a Portuguese family with benign hereditary chorea. 16220345 2005
CUI: C1859098
Disease: Chorea, Benign Familial
Chorea, Benign Familial 		0.300 GermlineCausalMutation disease ORPHANET Benign hereditary chorea: clinical, genetic, and pathological findings. 12891678 2003