Source: INFERRED

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: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C4025756
Disease: Abnormal aortic morphology
Abnormal aortic morphology
disease 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C4025211
Disease: Abnormal carotid artery morphology
Abnormal carotid artery morphology
disease 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C4020968
Disease: Abnormal localization of kidney
Abnormal localization of kidney
disease 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation
phenotype 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C3164445
Disease: Abnormality of aortic valve
Abnormality of aortic valve
disease 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
Abnormality of cardiovascular system morphology
disease 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C4551705
Disease: Abnormality of chromosome stability
Abnormality of chromosome stability
phenotype 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C4021750
Disease: Abnormality of femur morphology
Abnormality of femur morphology
disease 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
Abnormality of the hypothalamus-pituitary axis
disease 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver
phenotype 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C1846460
Disease: Abnormality of the outer ear
Abnormality of the outer ear
disease 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C4022016
Disease: Abnormality of the preputium
Abnormality of the preputium
disease 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C1405984
Disease: Absent radius
Absent radius
disease 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C0342526
Disease: Absent testes
Absent testes
phenotype 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C4024780
Disease: Almond-shaped palpebral fissure
Almond-shaped palpebral fissure
phenotype 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C0002871
Disease: Anemia
Anemia
disease 0.110 None 1.000 0 0 2017 2017
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C4025811
Disease: Anemic pallor
Anemic pallor
phenotype 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate
disease 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C4025071
Disease: Aplasia/Hypoplasia of fingers
Aplasia/Hypoplasia of fingers
phenotype 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C4024748
Disease: Aplasia/Hypoplasia of the iris
Aplasia/Hypoplasia of the iris
disease 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C2749463
Disease: Aplasia/Hypoplasia of the radius
Aplasia/Hypoplasia of the radius
phenotype 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C4023917
Disease: Aplasia/Hypoplasia of the uvula
Aplasia/Hypoplasia of the uvula
phenotype 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C0004106
Disease: Astigmatism
Astigmatism
disease 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
group 0.100 None 0 0
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C0004509
Disease: Azoospermia
Azoospermia
disease 0.100 None 0 0