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: C0151311
Disease: Cranial nerve palsies
Cranial nerve palsies 		0 1 0 0 1 1.00
CUI: C0242073
Disease: Pulmonary congestion
Pulmonary congestion 		0 1 0 0 1 1.00
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 1.00
CUI: C0272285
Disease: Heparin-induced thrombocytopenia
Heparin-induced thrombocytopenia 		0 5 0 0 1 0.20
CUI: C0002890
Disease: Leukoerythroblastic Anemia
Leukoerythroblastic Anemia 		1 1 1 1.00 1 1.00
CUI: C1328061
Disease: Myelodysplastic/myeloproliferative neoplasm, unclassifiable
Myelodysplastic/myeloproliferative neoplasm, unclassifiable 		1 1 1 1.00 1 1.00
CUI: C1516553
Disease: Prefibrotic/Early Primary Myelofibrosis
Prefibrotic/Early Primary Myelofibrosis 		1 1 1 1.00 1 1.00
CUI: C3281125
Disease: THROMBOCYTHEMIA 3
THROMBOCYTHEMIA 3 		1 1 1 1.00 1 1.00
CUI: C4016234
Disease: ERYTHROCYTOSIS, JAK2-RELATED, SOMATIC
ERYTHROCYTOSIS, JAK2-RELATED, SOMATIC 		1 0 1 1.00 0 0
CUI: C4303426
Disease: Refractory anemia with ringed sideroblasts associated with marked thrombocytosis
Refractory anemia with ringed sideroblasts associated with marked thrombocytosis 		1 1 1 1.00 1 1.00
CUI: C0003834
Disease: Arterial insufficiency
Arterial insufficiency 		2 0 1 0.50 0 0
CUI: C0025472
Disease: Mesenteric Vascular Occlusion
Mesenteric Vascular Occlusion 		3 0 1 0.33 0 0
CUI: C0027013
Disease: Myeloid Metaplasia
Myeloid Metaplasia 		3 1 1 0.33 1 1.00
CUI: C0232370
Disease: Florid red complexion (finding)
Florid red complexion (finding) 		3 0 1 0.33 0 0
CUI: C0677060
Disease: essential thrombocytopenia
essential thrombocytopenia 		3 0 1 0.33 0 0
CUI: C1849749
Disease: Peripheral thrombosis
Peripheral thrombosis 		3 0 1 0.33 0 0
CUI: C4273671
Disease: Inherited predisposition to essential thrombocythemia
Inherited predisposition to essential thrombocythemia 		3 0 1 0.33 0 0
CUI: C1268964
Disease: Myelodysplastic syndrome, no ICD-O subtype
Myelodysplastic syndrome, no ICD-O subtype 		4 0 1 0.25 0 0
CUI: C1334665
Disease: Mediastinal Lymphoma
Mediastinal Lymphoma 		4 0 1 0.25 0 0
CUI: C1853288
Disease: Increased red blood cell mass
Increased red blood cell mass 		4 0 1 0.25 0 0
CUI: C2347507
Disease: Childhood B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1
Childhood B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1 		4 0 1 0.25 0 0
CUI: C2827356
Disease: Myeloid/Lymphoid Neoplasms with Eosinophilia and Rearrangement of PDGFRA, PDGFRB, or FGFR1, or with PCM1-JAK2
Myeloid/Lymphoid Neoplasms with Eosinophilia and Rearrangement of PDGFRA, PDGFRB, or FGFR1, or with PCM1-JAK2 		4 0 1 0.25 0 0
CUI: C3805232
Disease: Post polycythaemia vera myelofibrosis
Post polycythaemia vera myelofibrosis 		4 1 1 0.25 1 1.00
CUI: C0153426
Disease: Malignant neoplasm of duodenum
Malignant neoplasm of duodenum 		5 1 1 0.20 1 1.00
CUI: C0239574
Disease: Low grade fever
Low grade fever 		5 0 1 0.20 0 0