Source: ALL
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: C2675212
Disease: Spherocytosis, Type 4
Spherocytosis, Type 4 		1 23 1 0.20 1 2.2E-02
CUI: C3161373
Disease: Dominant thalassemia
Dominant thalassemia 		1 0 1 0.20 0 0
CUI: C3274463
Disease: Sickle Beta 0 Thalassemia
Sickle Beta 0 Thalassemia 		1 0 1 0.20 0 0
CUI: C3280647
Disease: BACTEREMIA, SUSCEPTIBILITY TO, 2
BACTEREMIA, SUSCEPTIBILITY TO, 2 		1 1 1 0.20 1 4.3E-02
CUI: C3889873
Disease: HEMOGLOBIN SAINT ETIENNE PHENOTYPE
HEMOGLOBIN SAINT ETIENNE PHENOTYPE 		1 0 1 0.20 0 0
CUI: C3889898
Disease: HEMOGLOBIN C PHENOTYPE
HEMOGLOBIN C PHENOTYPE 		1 0 1 0.20 0 0
CUI: C3891694
Disease: HEMOGLOBIN TUBINGEN PHENOTYPE
HEMOGLOBIN TUBINGEN PHENOTYPE 		1 0 1 0.20 0 0
CUI: C4015898
Disease: RENAL TUBULAR ACIDOSIS, AUTOSOMAL DOMINANT
RENAL TUBULAR ACIDOSIS, AUTOSOMAL DOMINANT 		1 0 1 0.20 0 0
CUI: C4015903
Disease: SWANN BLOOD GROUP ANTIGEN PHENOTYPE
SWANN BLOOD GROUP ANTIGEN PHENOTYPE 		1 0 1 0.20 0 0
CUI: C4015904
Disease: ACANTHOCYTOSIS DUE TO BAND 3 HT
ACANTHOCYTOSIS DUE TO BAND 3 HT 		1 0 1 0.20 0 0
CUI: C4016175
Disease: HEMOGLOBIN HOUSTON PHENOTYPE
HEMOGLOBIN HOUSTON PHENOTYPE 		1 0 1 0.20 0 0
CUI: C4016522
Disease: G6PD TOMAH PHENOTYPE
G6PD TOMAH PHENOTYPE 		1 0 1 0.20 0 0
CUI: C4017494
Disease: BETA-KNOSSOS-THALASSEMIA
BETA-KNOSSOS-THALASSEMIA 		1 0 1 0.20 0 0
CUI: C4017510
Disease: BETA-MALAY-THALASSEMIA
BETA-MALAY-THALASSEMIA 		1 0 1 0.20 0 0
CUI: C4017522
Disease: BETA-SHOWA-YAKUSHIJI THALASSEMIA
BETA-SHOWA-YAKUSHIJI THALASSEMIA 		1 0 1 0.20 0 0
CUI: C4017525
Disease: BETA-PLUS-THALASSEMIA, DOMINANT
BETA-PLUS-THALASSEMIA, DOMINANT 		1 0 1 0.20 0 0
CUI: C4017528
Disease: BETA-THALASSEMIA, LERMONTOV TYPE
BETA-THALASSEMIA, LERMONTOV TYPE 		1 0 1 0.20 0 0
CUI: C4022665
Disease: Isothenuria
Isothenuria 		1 0 1 0.20 0 0
CUI: C4024695
Disease: Increased red cell sickling tendency
Increased red cell sickling tendency 		1 0 1 0.20 0 0
CUI: C4284047
Disease: HEMOGLOBIN AUBENAS PHENOTYPE
HEMOGLOBIN AUBENAS PHENOTYPE 		1 0 1 0.20 0 0
CUI: C4284050
Disease: HEMOGLOBIN GAMBARA PHENOTYPE
HEMOGLOBIN GAMBARA PHENOTYPE 		1 0 1 0.20 0 0
CUI: C4302087
Disease: Silent cerebral infarct
Silent cerebral infarct 		1 0 1 0.20 0 0
CUI: C4310971
Disease: HB NIIGATA
HB NIIGATA 		1 0 1 0.20 0 0
CUI: C4310973
Disease: BETA-THALASSEMIA INTERMEDIA, DOMINANT
BETA-THALASSEMIA INTERMEDIA, DOMINANT 		1 0 1 0.20 0 0
CUI: C4317046
Disease: Hematological abnormality
Hematological abnormality 		1 0 1 0.20 0 0