DisGeNET - a database of gene-disease associations

DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder), C1842342

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

Gene

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	3082
Gene Symbol:	HGF

HGF

0.600

Biomarker

disease

GENOMICS_ENGLAND

Targeted Next-Generation Sequencing Successfully Detects Causative Genes in Chinese Patients with Hereditary Hearing Loss.

2016

Entrez Id:	3082
Gene Symbol:	HGF

HGF

0.600

Biomarker

disease

CTD_human

Entrez Id:	3082
Gene Symbol:	HGF

HGF

0.600

CausalMutation

disease

CLINVAR