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: C0276196
Disease: Goatpox
Goatpox
1 0 1 2.6E-02 0 0
lip and oral cavity squamous cell carcinoma
1 0 1 2.6E-02 0 0
CUI: C0333419
Disease: Sarcoid type granuloma
Sarcoid type granuloma
1 0 1 2.6E-02 0 0
CUI: C0340324
Disease: Silent myocardial infarction
Silent myocardial infarction
1 0 1 2.6E-02 0 0
Granulomatous interstitial nephritis
1 0 1 2.6E-02 0 0
CUI: C0342444
Disease: Cyclical Cushing's syndrome
Cyclical Cushing's syndrome
1 0 1 2.6E-02 0 0
CUI: C0343400
Disease: Intestinal microsporidiosis
Intestinal microsporidiosis
1 0 1 2.6E-02 0 0
CUI: C0393992
Disease: Multicystic Encephalomalacia
Multicystic Encephalomalacia
1 0 1 2.6E-02 0 0
CUI: C0473221
Disease: Cryoglobulinemic glomerulonephritis
Cryoglobulinemic glomerulonephritis
1 0 1 2.6E-02 0 0
CUI: C0548823
Disease: Distress gastrointestinal
Distress gastrointestinal
1 0 1 2.6E-02 0 0
CUI: C0585187
Disease: Infected ascites
Infected ascites
1 0 1 2.6E-02 0 0
MPTP-Induced Degeneration of the Striatum
1 0 1 2.6E-02 0 0
Chronic proliferative glomerulonephritis
1 0 1 2.6E-02 0 0
CUI: C0856862
Disease: Posterior cerebral artery occlusion
Posterior cerebral artery occlusion
1 0 1 2.6E-02 0 0
CUI: C0861461
Disease: Stage IV Colon Carcinoma
Stage IV Colon Carcinoma
1 0 1 2.6E-02 0 0
CUI: C1291575
Disease: Deficiency of citrate(si)-synthase
Deficiency of citrate(si)-synthase
1 0 1 2.6E-02 0 0
CUI: C1334452
Disease: Neuroendocrine neoplasm of lung
Neuroendocrine neoplasm of lung
1 0 1 2.6E-02 0 0
CUI: C1335153
Disease: Ovarian Carcinoid Tumor
Ovarian Carcinoid Tumor
1 0 1 2.6E-02 0 0
CUI: C1535985
Disease: Staphylococcal osteomyelitis
Staphylococcal osteomyelitis
1 0 1 2.6E-02 0 0
CUI: C1697744
Disease: HIV peripheral neuropathy
HIV peripheral neuropathy
1 0 1 2.6E-02 0 0
Fetus affected by placental transfer of anticonvulsant
1 0 1 2.6E-02 0 0
CUI: C1841686
Disease: Absent hallux
Absent hallux
1 0 1 2.6E-02 0 0
CUI: C1852510
Disease: Craniofacial deafness hand syndrome
Craniofacial deafness hand syndrome
1 0 1 2.6E-02 0 0
CUI: C1855003
Disease: Bilateral postaxial polydactyly
Bilateral postaxial polydactyly
1 0 1 2.6E-02 0 0
CUI: C1856059
Disease: Mthfr Deficiency, Thermolabile Type
Mthfr Deficiency, Thermolabile Type
1 0 1 2.6E-02 0 0