DisGeNET - a database of gene-disease associations

TREM2, triggering receptor expressed on myeloid cells 2, 54209

N. diseases: 239; N. variants: 28

Disease: Semantic Dementia ×

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Disease

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

CUI:	C0338462
Disease:	Semantic Dementia

Semantic Dementia

0.400

SusceptibilityMutation

disease

ORPHANET

Heterozygous TREM2 mutations in frontotemporal dementia.

24139279

2014

CUI:	C0338462
Disease:	Semantic Dementia

Semantic Dementia

0.400

SusceptibilityMutation

disease

ORPHANET

Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes.

25042114

2014

CUI:	C0338462
Disease:	Semantic Dementia

Semantic Dementia

0.400

Biomarker

disease

HPO