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: C0311364
Disease: Anemia due to decreased red cell production
Anemia due to decreased red cell production 		1 0 1 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: C0221289
Disease: Synovioma, benign
Synovioma, benign 		2 0 1 0.11 0 0
CUI: C0424810
Disease: Periorbital swelling
Periorbital swelling 		2 0 1 0.11 0 0
CUI: C1266168
Disease: Malignant tenosynovial giant cell tumor
Malignant tenosynovial giant cell tumor 		2 0 1 0.11 0 0
CUI: C1394213
Disease: Crisis state
Crisis state 		2 0 1 0.11 0 0
CUI: C1516552
Disease: Overt Primary Myelofibrosis
Overt Primary Myelofibrosis 		2 0 1 0.11 0 0
CUI: C1845837
Disease: Dyserythropoietic Anemia with Thrombocytopenia
Dyserythropoietic Anemia with Thrombocytopenia 		2 0 1 0.11 0 0
CUI: C1860788
Disease: Transient Myeloproliferative Disorder of Down Syndrome
Transient Myeloproliferative Disorder of Down Syndrome 		2 0 1 0.11 0 0
CUI: C1867132
Disease: Plantar crease between first and second toes
Plantar crease between first and second toes 		2 0 1 0.11 0 0
CUI: C2931753
Disease: Achromatopsia incomplete, X-linked
Achromatopsia incomplete, X-linked 		2 0 1 0.11 0 0
CUI: C3150926
Disease: Congenital dyserythropoietic anemia type IV
Congenital dyserythropoietic anemia type IV 		2 0 1 0.11 0 0
CUI: C3887937
Disease: CONE DYSTROPHY 5, X-LINKED
CONE DYSTROPHY 5, X-LINKED 		2 0 1 0.11 0 0
CUI: C4023024
Disease: Abnormality of multiple cell lineages in the bone marrow
Abnormality of multiple cell lineages in the bone marrow 		2 0 1 0.11 0 0
CUI: C4025806
Disease: High axial triradius
High axial triradius 		2 0 1 0.11 0 0