Gene: FANCB ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2187
Gene Symbol: FANCB
FANCB 		0.620 Biomarker disease GENOMICS_ENGLAND X-linked recessive VACTERL-H due to a mutation in FANCB in a preterm boy. 26683739 2016
Entrez Id: 2187
Gene Symbol: FANCB
FANCB 		0.620 GeneticVariation disease BEFREE X-linked VACTERL-hydrocephalus syndrome (X-linked VACTERL-H) is a rare disorder caused by mutations in the gene FANCB which underlies Fanconi Anemia (FA) complementation group B. 21910217 2011
Entrez Id: 2187
Gene Symbol: FANCB
FANCB 		0.620 GermlineCausalMutation disease ORPHANET X-linked VACTERL-hydrocephalus syndrome (X-linked VACTERL-H) is a rare disorder caused by mutations in the gene FANCB which underlies Fanconi Anemia (FA) complementation group B. 21910217 2011
Entrez Id: 2187
Gene Symbol: FANCB
FANCB 		0.620 GeneticVariation disease BEFREE To determine if mutations in FANCB, which are known to cause Fanconi anaemia complementation group B, are a cause of X linked VACTERL-H syndrome. 16679491 2006
Entrez Id: 2187
Gene Symbol: FANCB
FANCB 		0.620 Biomarker disease GENOMICS_ENGLAND X-linked inheritance of Fanconi anemia complementation group B. 15502827 2004
Entrez Id: 2187
Gene Symbol: FANCB
FANCB 		0.620 Biomarker disease CTD_human