Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 2.8E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE
0 1 0 0 1 2.8E-02
CUI: C0852711
Disease: Sickle Cell Dactylitis
Sickle Cell Dactylitis
0 7 0 0 1 2.4E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0 9 0 0 1 2.3E-02
CUI: C1969810
Disease: FEBRILE CONVULSIONS, FAMILIAL, 8
FEBRILE CONVULSIONS, FAMILIAL, 8
0 13 0 0 1 2.1E-02
CUI: C3890602
Disease: Bodily Pain
Bodily Pain
0 4 0 0 1 2.6E-02
CUI: C0016479
Disease: Food Poisoning
Food Poisoning
1 0 1 1.1E-02 0 0
CUI: C0036749
Disease: Serositis
Serositis
1 0 1 1.1E-02 0 0
CUI: C0042907
Disease: Vitreous Detachment
Vitreous Detachment
1 0 1 1.1E-02 0 0
CUI: C0086240
Disease: Epilepsy, Simple Partial
Epilepsy, Simple Partial
1 0 1 1.1E-02 0 0
CUI: C0153261
Disease: Histoplasma capsulatum Infection
Histoplasma capsulatum Infection
1 0 1 1.1E-02 0 0
CUI: C0154565
Disease: Non-organic sleep disorder
Non-organic sleep disorder
1 0 1 1.1E-02 0 0
CUI: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia
1 0 1 1.1E-02 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia
1 0 1 1.1E-02 0 0
CUI: C0234461
Disease: aphasic
aphasic
1 0 1 1.1E-02 0 0
CUI: C0234516
Disease: Speech dysfunction
Speech dysfunction
1 0 1 1.1E-02 0 0
CUI: C0241831
Disease: Cerebral salt-wasting syndrome
Cerebral salt-wasting syndrome
1 0 1 1.1E-02 0 0
CUI: C0264939
Disease: Systemic Vasculitis
Systemic Vasculitis
1 0 1 1.1E-02 0 0
CUI: C0267448
Disease: Eosinophilic colitis
Eosinophilic colitis
1 0 1 1.1E-02 0 0
CUI: C0270847
Disease: Benign Focal Epilepsy, Childhood
Benign Focal Epilepsy, Childhood
1 0 1 1.1E-02 0 0
CUI: C0271428
Disease: Disorder of middle ear
Disorder of middle ear
1 0 1 1.1E-02 0 0
CUI: C0280242
Disease: stage, rectal cancer
stage, rectal cancer
1 0 1 1.1E-02 0 0
CUI: C0338483
Disease: Migraine with Prolonged Aura
Migraine with Prolonged Aura
1 0 1 1.1E-02 0 0
Conduct disorder, childhood-onset type
1 0 1 1.1E-02 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia
1 0 1 1.1E-02 0 0