DisGeNET - a database of gene-disease associations

Source: HPO

Disease: Cerebral cortical atrophy ×

Gene: PRDM16 ×

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

Gene

Gene Full Name

DSI _g

DPI _g

pLI

Disease

Type

Score _gda

EL_gda

EI _gda

N.PMIDs

N.SNPs _gda

First Ref.

LastRef.

Entrez Id:	63976
Gene Symbol:	PRDM16

PRDM16

PR/SET domain 16

0.522

0.808

1.00

CUI:	C4551583
Disease:	Cerebral cortical atrophy

Cerebral cortical atrophy

disease

0.100

None

0