Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10459
Gene Symbol: MAD2L2
MAD2L2
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia
0.510 GermlineCausalMutation ORPHANET Finally, silencing Rev7 in primary hematopoietic cells impaired progenitor function, suggesting that the DNA repair defect underlies the development of BMF in FA. 27500492

2016