Source: CURATED ×
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic 		13 0 4 0.20 0 0
CUI: C0002879
Disease: Anemia, Hemolytic, Acquired
Anemia, Hemolytic, Acquired 		13 0 4 0.20 0 0
CUI: C0002889
Disease: Anemia, Microangiopathic
Anemia, Microangiopathic 		13 0 4 0.20 0 0
CUI: C0221021
Disease: Microangiopathic hemolytic anemia
Microangiopathic hemolytic anemia 		13 0 4 0.20 0 0
CUI: C0002882
Disease: Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Hemolytic, Congenital Nonspherocytic 		3 0 2 0.17 0 0
CUI: C0010074
Disease: Coronary Vessel Anomalies
Coronary Vessel Anomalies 		1 0 1 9.1E-02 0 0
CUI: C0015702
Disease: Favism
Favism 		1 0 1 9.1E-02 0 0
CUI: C0031306
Disease: Phagocyte Bactericidal Dysfunction
Phagocyte Bactericidal Dysfunction 		1 0 1 9.1E-02 0 0
CUI: C0268523
Disease: Glutamate-cysteine ligase deficiency
Glutamate-cysteine ligase deficiency 		1 0 1 9.1E-02 0 0
CUI: C0272066
Disease: Glycogen Storage Disease XII
Glycogen Storage Disease XII 		1 0 1 9.1E-02 0 0
CUI: C0340968
Disease: Deficiency of pyruvate kinase
Deficiency of pyruvate kinase 		1 0 1 9.1E-02 0 0
CUI: C0398562
Disease: Triose phosphate isomerase deficiency
Triose phosphate isomerase deficiency 		1 0 1 9.1E-02 0 0
CUI: C0398746
Disease: Gluthathione synthetase deficiency
Gluthathione synthetase deficiency 		1 0 1 9.1E-02 0 0
CUI: C0472792
Disease: Hemolytic anemia due to hexokinase deficiency
Hemolytic anemia due to hexokinase deficiency 		1 0 1 9.1E-02 0 0
CUI: C1854449
Disease: Neuropathy, hereditary motor and sensory, Russe type
Neuropathy, hereditary motor and sensory, Russe type 		1 0 1 9.1E-02 0 0
CUI: C1856399
Disease: Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to
Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to 		1 0 1 9.1E-02 0 0
CUI: C1856603
Disease: Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to 		1 0 1 9.1E-02 0 0
CUI: C1860808
Disease: Triosephosphate Isomerase Deficiency
Triosephosphate Isomerase Deficiency 		1 0 1 9.1E-02 0 0
CUI: C1863224
Disease: Adenosine Triphosphate, Elevated, Of Erythrocytes
Adenosine Triphosphate, Elevated, Of Erythrocytes 		1 0 1 9.1E-02 0 0
CUI: C2939465
Disease: Deficiency of glucose-6-phosphate dehydrogenase
Deficiency of glucose-6-phosphate dehydrogenase 		1 0 1 9.1E-02 0 0
CUI: C3150343
Disease: HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY
HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY 		1 0 1 9.1E-02 0 0
CUI: C3809513
Disease: AORTIC ANEURYSM, FAMILIAL THORACIC 8
AORTIC ANEURYSM, FAMILIAL THORACIC 8 		1 0 1 9.1E-02 0 0
CUI: C4479526
Disease: RETINITIS PIGMENTOSA 79
RETINITIS PIGMENTOSA 79 		1 0 1 9.1E-02 0 0
CUI: C0002735
Disease: Oppenheim's Disease
Oppenheim's Disease 		2 0 1 8.3E-02 0 0
CUI: C0027868
Disease: Neuromuscular Diseases
Neuromuscular Diseases 		2 0 1 8.3E-02 0 0