Source: GENOMICS_ENGLAND

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 2176
Gene Symbol: FANCC
FANCC 		FA complementation group C 0.507 0.808 2.8E-13
CUI: C3468041
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP C
FANCONI ANEMIA, COMPLEMENTATION GROUP C 		disease 0.950 definitive 1.000 5 0 1992 2018
Entrez Id: 2176
Gene Symbol: FANCC
FANCC 		FA complementation group C 0.507 0.808 2.8E-13
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia 		disease 0.700 strong 1.000 4 0 1992 2019
Entrez Id: 2176
Gene Symbol: FANCC
FANCC 		FA complementation group C 0.507 0.808 2.8E-13
CUI: C0023418
Disease: leukemia
leukemia 		disease 0.610 strong 1.000 1 0 2008 2016
Entrez Id: 2176
Gene Symbol: FANCC
FANCC 		FA complementation group C 0.507 0.808 2.8E-13
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		disease 0.520 strong 1.000 1 0 2003 2016
Entrez Id: 2176
Gene Symbol: FANCC
FANCC 		FA complementation group C 0.507 0.808 2.8E-13
CUI: C0030312
Disease: Pancytopenia
Pancytopenia 		disease 0.410 strong 1.000 3 0 1992 2016
Entrez Id: 2176
Gene Symbol: FANCC
FANCC 		FA complementation group C 0.507 0.808 2.8E-13
CUI: C1384666
Disease: hearing impairment
hearing impairment 		phenotype 0.400 strong 1.000 2 0 1992 2006
Entrez Id: 2176
Gene Symbol: FANCC
FANCC 		FA complementation group C 0.507 0.808 2.8E-13
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME 		group 0.400 strong 1.000 1 0 2016 2016
Entrez Id: 2176
Gene Symbol: FANCC
FANCC 		FA complementation group C 0.507 0.808 2.8E-13
CUI: C1855710
Disease: Bone marrow hypocellularity
Bone marrow hypocellularity 		phenotype 0.300 strong 1.000 3 0 1992 2016
Entrez Id: 2176
Gene Symbol: FANCC
FANCC 		FA complementation group C 0.507 0.808 2.8E-13
CUI: C2750866
Disease: Growth retardation, pre- and postnatal
Growth retardation, pre- and postnatal 		phenotype 0.300 strong 1.000 2 0 1992 2006
Entrez Id: 2176
Gene Symbol: FANCC
FANCC 		FA complementation group C 0.507 0.808 2.8E-13
CUI: C4228778
Disease: Abnormality of radial ray
Abnormality of radial ray 		phenotype 0.300 strong 1.000 1 0 1992 1992
Entrez Id: 2176
Gene Symbol: FANCC
FANCC 		FA complementation group C 0.507 0.808 2.8E-13
CUI: C0265219
Disease: Miller Dieker syndrome
Miller Dieker syndrome 		disease 0.300 strong 1.000 1 0 2016 2016
Entrez Id: 2176
Gene Symbol: FANCC
FANCC 		FA complementation group C 0.507 0.808 2.8E-13
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia 		disease 0.300 strong 1.000 1 0 2016 2016
Entrez Id: 2176
Gene Symbol: FANCC
FANCC 		FA complementation group C 0.507 0.808 2.8E-13
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm 		disease 0.300 strong 0 0