DisGeNET - a database of gene-disease associations

Source: CTD_human

Disease: Profound Mental Retardation ×

Gene: DEAF1 ×

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

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	10522
Gene Symbol:	DEAF1

DEAF1

CUI:	C0020796
Disease:	Profound Mental Retardation

Profound Mental Retardation

0.300

Biomarker

CTD_human

A de novo paradigm for mental retardation.

2010