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: C3887980
Disease: Protanomaly
Protanomaly 		19 0 5 0.23 0 0
CUI: C0036211
Disease: Sarcoma 180
Sarcoma 180 		20 0 5 0.22 0 0
CUI: C4076240
Disease: Chronic kidney disease mineral and bone disorder
Chronic kidney disease mineral and bone disorder 		26 0 5 0.17 0 0
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		29 0 5 0.16 0 0
CUI: C2825306
Disease: Treatment related leukaemia
Treatment related leukaemia 		30 0 5 0.15 0 0
CUI: C0035934
Disease: Rubinstein-Taybi Syndrome
Rubinstein-Taybi Syndrome 		31 0 5 0.15 0 0
CUI: C0242225
Disease: Color blindness
Color blindness 		33 0 5 0.14 0 0
CUI: C0032339
Disease: Rothmund-Thomson syndrome
Rothmund-Thomson syndrome 		35 0 5 0.13 0 0
CUI: C3831784
Disease: Acute monocytic/monoblastic leukemia
Acute monocytic/monoblastic leukemia 		35 0 5 0.13 0 0
CUI: C0311364
Disease: Anemia due to decreased red cell production
Anemia due to decreased red cell production 		1 0 1 0.12 0 0
CUI: C0457334
Disease: Acute monoblastic leukemia
Acute monoblastic leukemia 		37 0 5 0.12 0 0
CUI: C1839161
Disease: Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis 		1 0 1 0.12 0 0
CUI: C1866810
Disease: ELLIPTOCYTOSIS 3
ELLIPTOCYTOSIS 3 		1 9 1 0.12 1 4.8E-02
CUI: C2826104
Disease: Myeloid Proliferations Associated with Down Syndrome
Myeloid Proliferations Associated with Down Syndrome 		1 0 1 0.12 0 0
CUI: C3267190
Disease: Fetal thrombotic vasculopathy
Fetal thrombotic vasculopathy 		1 0 1 0.12 0 0
CUI: C3502510
Disease: Chromosome 16p13.3 Deletion Syndrome
Chromosome 16p13.3 Deletion Syndrome 		1 0 1 0.12 0 0
CUI: C3550789
Disease: THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA
THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA 		1 0 1 0.12 0 0
CUI: C3550856
Disease: ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES
ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES 		1 0 1 0.12 0 0
CUI: C4016380
Disease: ANEMIA, PERINATAL HEMOLYTIC, FATAL OR NEAR-FATAL
ANEMIA, PERINATAL HEMOLYTIC, FATAL OR NEAR-FATAL 		1 0 1 0.12 0 0
CUI: C4016507
Disease: THROMBOCYTOPENIA, X-LINKED, WITH DYSERYTHROPOIETIC ANEMIA
THROMBOCYTOPENIA, X-LINKED, WITH DYSERYTHROPOIETIC ANEMIA 		1 0 1 0.12 0 0
CUI: C4016508
Disease: THROMBOCYTOPENIA, X-LINKED, WITHOUT DYSERYTHROPOIETIC ANEMIA
THROMBOCYTOPENIA, X-LINKED, WITHOUT DYSERYTHROPOIETIC ANEMIA 		1 0 1 0.12 0 0
CUI: C4477036
Disease: Abnormal location of the eyebrow
Abnormal location of the eyebrow 		1 0 1 0.12 0 0
CUI: C0302486
Disease: Erythrophagocytosis
Erythrophagocytosis 		40 0 5 0.12 0 0
CUI: C4688007
Disease: Platinum-Resistant Ovarian Carcinoma
Platinum-Resistant Ovarian Carcinoma 		41 0 5 0.11 0 0
CUI: C0221289
Disease: Synovioma, benign
Synovioma, benign 		2 0 1 0.11 0 0