DisGeNET - a database of gene-disease associations

Gene: FANCB ×

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:	2187
Gene Symbol:	FANCB

FANCB

CUI:	C1848600
Disease:	Vater Association With Hydrocephalus

Vater Association With Hydrocephalus

0.300

GermlineCausalMutation

ORPHANET

X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations.

2011