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: C3894553
Disease: response to simvastatin
response to simvastatin
21 0 1 4.0E-02 0 0
CUI: C0233844
Disease: Clumsiness
Clumsiness
48 0 2 3.9E-02 0 0
CUI: C0334607
Disease: Psammomatous Meningioma
Psammomatous Meningioma
22 0 1 3.8E-02 0 0
CUI: C0162672
Disease: MERRF Syndrome
MERRF Syndrome
51 0 2 3.7E-02 0 0
CUI: C0270764
Disease: Motor Neuron Disease, Lower
Motor Neuron Disease, Lower
23 0 1 3.7E-02 0 0
CUI: C0685787
Disease: Cleft face
Cleft face
23 0 1 3.7E-02 0 0
CUI: C1849508
Disease: EPILEPSY, PYRIDOXINE-DEPENDENT
EPILEPSY, PYRIDOXINE-DEPENDENT
25 0 1 3.4E-02 0 0
CUI: C0018915
Disease: Hemangioendothelioma
Hemangioendothelioma
26 0 1 3.3E-02 0 0
CUI: C3887612
Disease: Psychomotor Agitation
Psychomotor Agitation
26 0 1 3.3E-02 0 0
CUI: C0019087
Disease: Hemorrhagic Disorders
Hemorrhagic Disorders
30 0 1 2.9E-02 0 0
CUI: C4021757
Disease: EEG with polyspike wave complexes
EEG with polyspike wave complexes
30 0 1 2.9E-02 0 0
CUI: C0018781
Disease: Noise-induced hearing loss
Noise-induced hearing loss
33 0 1 2.7E-02 0 0
CUI: C0281784
Disease: Benign Meningioma
Benign Meningioma
35 0 1 2.6E-02 0 0
CUI: C0030389
Disease: Parainfluenza
Parainfluenza
36 0 1 2.5E-02 0 0
CUI: C1839364
Disease: Progressive visual loss
Progressive visual loss
77 0 2 2.5E-02 0 0
CUI: C0349604
Disease: Intracranial Meningioma
Intracranial Meningioma
38 0 1 2.4E-02 0 0
CUI: C3711376
Disease: Isodicentric Chromosome 15 Syndrome
Isodicentric Chromosome 15 Syndrome
39 0 1 2.3E-02 0 0
CUI: C0241816
Disease: Global brain atrophy
Global brain atrophy
41 0 1 2.2E-02 0 0
Complex partial seizure with impairment of consciousness
41 0 1 2.2E-02 0 0
Degenerative Diseases, Central Nervous System
43 0 1 2.1E-02 0 0
CUI: C0751783
Disease: Lafora Disease
Lafora Disease
92 0 2 2.1E-02 0 0
Adult Pre-B Acute Lymphoblastic Leukemia
44 0 1 2.1E-02 0 0
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms
45 0 1 2.0E-02 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic
46 0 1 2.0E-02 0 0
CUI: C0751778
Disease: Myoclonic Epilepsies, Progressive
Myoclonic Epilepsies, Progressive
48 0 1 1.9E-02 0 0