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: C0393484
Disease: Rasmussen Syndrome
Rasmussen Syndrome
18 3 15 0.75 1 0.33
CUI: C0948853
Disease: Euthymia
Euthymia
10 0 3 0.12 0 0
CUI: C0235165
Disease: Mania acute
Mania acute
2 0 2 0.12 0 0
CUI: C0338715
Disease: Drug-induced depressive state
Drug-induced depressive state
13 0 3 0.11 0 0
CUI: C0034189
Disease: Pyemia
Pyemia
24 0 4 0.11 0 0
Proliferative diabetic retinopathy - quiescent
6 0 2 9.5E-02 0 0
CUI: C0014549
Disease: Tonic-Clonic Epilepsy
Tonic-Clonic Epilepsy
19 0 3 9.1E-02 0 0
CUI: C0020435
Disease: Hyperbilirubinemia, Hereditary
Hyperbilirubinemia, Hereditary
8 0 2 8.7E-02 0 0
CUI: C1275465
Disease: Tumor stage mycosis fungoides
Tumor stage mycosis fungoides
8 0 2 8.7E-02 0 0
CUI: C1449647
Disease: Secondary Peritonitis
Secondary Peritonitis
8 0 2 8.7E-02 0 0
Acute encephalopathy with biphasic seizures and late reduced diffusion
8 0 2 8.7E-02 0 0
CUI: C0043121
Disease: Wernicke Encephalopathy
Wernicke Encephalopathy
9 0 2 8.3E-02 0 0
CUI: C0271454
Disease: Chronic purulent otitis media
Chronic purulent otitis media
9 0 2 8.3E-02 0 0
CUI: C0854119
Disease: Ruptured Appendicitis
Ruptured Appendicitis
9 0 2 8.3E-02 0 0
CUI: C0857501
Disease: Acute schizophrenia
Acute schizophrenia
9 0 2 8.3E-02 0 0
atopic eczema/dermatitis (non-specific)
10 0 2 8.0E-02 0 0
CUI: C0751117
Disease: Cryptogenic Tonic-Clonic Epilepsy
Cryptogenic Tonic-Clonic Epilepsy
10 0 2 8.0E-02 0 0
CUI: C0751118
Disease: Epilepsy, Tonic-Clonic, Familial
Epilepsy, Tonic-Clonic, Familial
10 0 2 8.0E-02 0 0
CUI: C0751119
Disease: Epilepsy, Tonic-Clonic, Symptomatic
Epilepsy, Tonic-Clonic, Symptomatic
10 0 2 8.0E-02 0 0
CUI: C0018188
Disease: Granuloma
Granuloma
24 0 3 7.9E-02 0 0
CUI: C0008513
Disease: Chorioretinitis
Chorioretinitis
11 0 2 7.7E-02 0 0
CUI: C0242973
Disease: Ventricular Dysfunction
Ventricular Dysfunction
11 0 2 7.7E-02 0 0
CUI: C0729552
Disease: Genital infection
Genital infection
11 0 2 7.7E-02 0 0
CUI: C1335392
Disease: Pericytic Neoplasm
Pericytic Neoplasm
11 0 2 7.7E-02 0 0
HYPERTRICHOSIS, CONGENITAL GENERALIZED
25 0 3 7.7E-02 0 0