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: C0424810
Disease: Periorbital swelling
Periorbital swelling 		2 0 1 0.11 0 0
CUI: C0427480
Disease: Elliptocytosis found
Elliptocytosis found 		12 0 2 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: C1292780
Disease: Therapy-related myelodysplastic syndrome
Therapy-related myelodysplastic syndrome 		42 0 5 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
CUI: C4511003
Disease: Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Acute myeloid leukemia with t(8;16)(p11;p13) translocation 		2 0 1 0.11 0 0
CUI: C4551859
Disease: RUBINSTEIN-TAYBI SYNDROME 1
RUBINSTEIN-TAYBI SYNDROME 1 		2 0 1 0.11 0 0
CUI: C0235813
Disease: Neonatal leukaemia
Neonatal leukaemia 		3 0 1 1.0E-01 0 0
CUI: C1290508
Disease: Abnormal number of teeth
Abnormal number of teeth 		3 0 1 1.0E-01 0 0
CUI: C1542667
Disease: Congenital erythroid hypoplasia
Congenital erythroid hypoplasia 		3 0 1 1.0E-01 0 0
CUI: C1864828
Disease: ALZHEIMER DISEASE 10
ALZHEIMER DISEASE 10 		3 0 1 1.0E-01 0 0
CUI: C2718078
Disease: Deficiency of Uroporphyrinogen III Synthase
Deficiency of Uroporphyrinogen III Synthase 		3 0 1 1.0E-01 0 0
CUI: C4025111
Disease: Radial deviation of thumb terminal phalanx
Radial deviation of thumb terminal phalanx 		3 0 1 1.0E-01 0 0
CUI: C4551635
Disease: Deuteranopia
Deuteranopia 		3 0 1 1.0E-01 0 0
CUI: C0598894
Disease: Monocytic leukemia
Monocytic leukemia 		71 0 7 9.7E-02 0 0
CUI: C0008928
Disease: Cleidocranial Dysplasia
Cleidocranial Dysplasia 		52 0 5 9.1E-02 0 0