Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55159
Gene Symbol: RFWD3
RFWD3
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia 		0.320 GermlineCausalMutation ORPHANET Although RFWD3 mutations have thus far been detected in a single child with FA, we propose RFWD3 as an FA gene, FANCW, supported by cellular paradigm systems and an animal model. 28691929

2017