Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
FANCONI ANEMIA, COMPLEMENTATION GROUP N
0.710 Biomarker disease CLINGEN Inactivation of Palb2 gene leads to mesoderm differentiation defect and early embryonic lethality in mice. 20484223 2010
FANCONI ANEMIA, COMPLEMENTATION GROUP N
0.710 Biomarker disease GENOMICS_ENGLAND
FANCONI ANEMIA, COMPLEMENTATION GROUP N
0.710 Biomarker disease CLINGEN Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. 17200671 2007
FANCONI ANEMIA, COMPLEMENTATION GROUP N
0.710 Biomarker disease CLINGEN Fanconi anaemia and cancer: an intricate relationship. 29376519 2018
FANCONI ANEMIA, COMPLEMENTATION GROUP N
0.710 Biomarker disease CLINGEN Fanconi anemia is associated with a defect in the BRCA2 partner PALB2. 17200672 2007
FANCONI ANEMIA, COMPLEMENTATION GROUP N
0.710 Biomarker disease GENOMICS_ENGLAND Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. 17200671 2007
FANCONI ANEMIA, COMPLEMENTATION GROUP N
0.710 CausalMutation disease CLINVAR
FANCONI ANEMIA, COMPLEMENTATION GROUP N
0.710 Biomarker disease CLINGEN ChAM, a novel motif that mediates PALB2 intrinsic chromatin binding and facilitates DNA repair. 22193777 2012
FANCONI ANEMIA, COMPLEMENTATION GROUP N
0.710 Biomarker disease GENOMICS_ENGLAND
FANCONI ANEMIA, COMPLEMENTATION GROUP N
0.710 Biomarker disease CTD_human
FANCONI ANEMIA, COMPLEMENTATION GROUP N
0.710 Biomarker disease GENOMICS_ENGLAND Fanconi anemia is associated with a defect in the BRCA2 partner PALB2. 17200672 2007
FANCONI ANEMIA, COMPLEMENTATION GROUP N
0.710 Biomarker disease BEFREE Fanconi anemia (FA) associated genes [FANCA, -B, -C, FANCD1(BRCA2), -D2, -E, -F, -G, -I, -L, -M, FANCN (PALB2), FANCJ(BRIP1) and FA-linked BRCA1] encode proteins of DNA damage response pathways mutated in FA patients. 21567085 2011