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: C0522070
Disease: Pancreatic symptom
Pancreatic symptom
5 0 1 0.17 0 0
CUI: C3150902
Disease: C1q DEFICIENCY
C1q DEFICIENCY
5 0 1 0.17 0 0
CUI: C3666017
Disease: Cholangiopathy
Cholangiopathy
6 0 1 0.14 0 0
Multiple small medullary renal cysts
6 0 1 0.14 0 0
CUI: C4025744
Disease: Foot acroosteolysis
Foot acroosteolysis
6 0 1 0.14 0 0
CUI: C0155120
Disease: Corneal Dystrophy, Band-Shaped
Corneal Dystrophy, Band-Shaped
7 0 1 0.12 0 0
CUI: C0266548
Disease: Axenfeld anomaly (disorder)
Axenfeld anomaly (disorder)
7 0 1 0.12 0 0
SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 2
7 0 1 0.12 0 0
CUI: C0332886
Disease: Coarctation
Coarctation
8 0 1 0.11 0 0
CUI: C0334584
Disease: Spongioblastoma
Spongioblastoma
8 0 1 0.11 0 0
Cerebral Primitive Neuroectodermal Tumor
9 0 1 1.0E-01 0 0
CUI: C1855284
Disease: Intrahepatic biliary atresia
Intrahepatic biliary atresia
9 0 1 1.0E-01 0 0
CUI: C1855669
Disease: Absent frontal sinuses
Absent frontal sinuses
9 0 1 1.0E-01 0 0
CUI: C4025573
Disease: Increased muscle fatiguability
Increased muscle fatiguability
9 0 1 1.0E-01 0 0
CUI: C0282631
Disease: Facies
Facies
10 0 1 9.1E-02 0 0
CUI: C0948368
Disease: Kaufman-McKusick syndrome
Kaufman-McKusick syndrome
10 0 1 9.1E-02 0 0
Peripheral pulmonary artery stenosis
23 0 2 8.7E-02 0 0
CUI: C0423808
Disease: Brachyonychia
Brachyonychia
11 0 1 8.3E-02 0 0
CUI: C1839454
Disease: PROPERDIN DEFICIENCY, X-LINKED
PROPERDIN DEFICIENCY, X-LINKED
11 0 1 8.3E-02 0 0
CUI: C0206653
Disease: Angiomyoma
Angiomyoma
12 0 1 7.7E-02 0 0
CUI: C0334596
Disease: Medulloepithelioma
Medulloepithelioma
13 0 1 7.1E-02 0 0
CUI: C4072904
Disease: Secondary Caesarian section
Secondary Caesarian section
13 0 1 7.1E-02 0 0
CUI: C1839798
Disease: Long nose
Long nose
29 0 2 6.9E-02 0 0
CUI: C0154017
Disease: Benign neoplasm of bladder
Benign neoplasm of bladder
15 0 1 6.2E-02 0 0
Neoplasm of uncertain or unknown behavior of bladder
15 0 1 6.2E-02 0 0