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: C1304508
Disease: Spindle cell hemangioma
Spindle cell hemangioma
68 0 11 0.10 0 0
Solid pseudopapillary tumour of the pancreas
9 0 4 7.0E-02 0 0
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder)
40 0 6 7.0E-02 0 0
Refractory anemia with excess blasts in transformation (clinical)
10 0 4 6.9E-02 0 0
CUI: C0267375
Disease: Chronic colitis
Chronic colitis
57 0 7 6.9E-02 0 0
CUI: C1565321
Disease: Cholera Infantum
Cholera Infantum
12 0 4 6.7E-02 0 0
CUI: C0085702
Disease: Monocytosis
Monocytosis
61 0 7 6.6E-02 0 0
CUI: C0151857
Disease: Pleocytosis
Pleocytosis
31 0 5 6.4E-02 0 0
CUI: C1853118
Disease: Severe congenital neutropenia
Severe congenital neutropenia
66 26 7 6.3E-02 1 2.6E-02
CUI: C0155686
Disease: Acute myocarditis
Acute myocarditis
33 0 5 6.2E-02 0 0
CUI: C0340970
Disease: Congenital neutropenia
Congenital neutropenia
68 11 7 6.2E-02 1 4.2E-02
CUI: C0010324
Disease: Crigler Najjar syndrome, type 1
Crigler Najjar syndrome, type 1
17 0 4 6.2E-02 0 0
Extramedullary Hematopoiesis (disorder)
52 0 6 6.1E-02 0 0
CUI: C0279646
Disease: Childhood Acute Monocytic Leukemia
Childhood Acute Monocytic Leukemia
70 0 7 6.1E-02 0 0
CUI: C0280634
Disease: Adult Acute Monocytic Leukemia
Adult Acute Monocytic Leukemia
70 0 7 6.1E-02 0 0
CUI: C0740985
Disease: Acute anaemia
Acute anaemia
18 0 4 6.1E-02 0 0
Endometrial Endometrioid Adenocarcinoma
53 0 6 6.1E-02 0 0
CUI: C1850383
Disease: Neuropathy, Painful
Neuropathy, Painful
18 0 4 6.1E-02 0 0
CUI: C4528176
Disease: High Risk Myelodysplastic Syndrome
High Risk Myelodysplastic Syndrome
19 0 4 6.0E-02 0 0
CUI: C0334121
Disease: Inflammatory Myofibroblastic Tumor
Inflammatory Myofibroblastic Tumor
92 0 8 5.9E-02 0 0
CUI: C0347129
Disease: Dysplasia of anus
Dysplasia of anus
21 0 4 5.8E-02 0 0
CUI: C4324336
Disease: Hyperleukocytosis
Hyperleukocytosis
21 0 4 5.8E-02 0 0
CUI: C0020433
Disease: Hyperbilirubinemia
Hyperbilirubinemia
131 0 10 5.8E-02 0 0
CUI: C0175697
Disease: Van der Woude syndrome
Van der Woude syndrome
113 0 9 5.8E-02 0 0
Neonatal Systemic lupus erythematosus
22 0 4 5.7E-02 0 0