Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0003113
Disease: Anomia
Anomia 		0.110 GeneticVariation BEFREE Progressive anomia revisited: focal degeneration associated with progranulin gene mutation. 18781435

2007
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0003113
Disease: Anomia
Anomia 		0.110 Biomarker HPO

Entrez Id: 54664
Gene Symbol: TMEM106B
TMEM106B
CUI: C0003113
Disease: Anomia
Anomia 		0.100 Biomarker HPO

Entrez Id: 25978
Gene Symbol: CHMP2B
CHMP2B
CUI: C0003113
Disease: Anomia
Anomia 		0.100 Biomarker HPO

Entrez Id: 54209
Gene Symbol: TREM2
TREM2
CUI: C0003113
Disease: Anomia
Anomia 		0.100 Biomarker HPO

Entrez Id: 5663
Gene Symbol: PSEN1
PSEN1
CUI: C0003113
Disease: Anomia
Anomia 		0.100 Biomarker HPO

Entrez Id: 4137
Gene Symbol: MAPT
MAPT
CUI: C0003113
Disease: Anomia
Anomia 		0.100 Biomarker HPO

Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72
CUI: C0003113
Disease: Anomia
Anomia 		0.100 Biomarker HPO

Entrez Id: 348
Gene Symbol: APOE
APOE
CUI: C0003113
Disease: Anomia
Anomia 		0.010 Biomarker BEFREE The increase in tau H2 haplotype frequency (50.0%) is especially pronounced in patients with AA who are APOE epsilon4 positive compared with patients with FD (18.8%, P=.04), patients with AD (24.8%, P=.005), and cognitively normal patients (15.3%, P<.001).APOE epsilon4 and tau H2 haplotype frequencies are not significantly different in patients with FD and PA compared with healthy patients. 11939896

2002