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: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
577 0 1 1.7E-03 0 0
CUI: C0002170
Disease: Alopecia
Alopecia
491 0 1 2.0E-03 0 0
CUI: C0205710
Disease: Alpers Syndrome (disorder)
Alpers Syndrome (disorder)
28 0 1 2.6E-02 0 0
CUI: C0034219
Disease: Alveolar pyorrhea
Alveolar pyorrhea
2 0 1 7.7E-02 0 0
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
3397 0 1 2.9E-04 0 0
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
1114 0 1 8.9E-04 0 0
CUI: C0002871
Disease: Anemia
Anemia
847 0 1 1.2E-03 0 0
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell
434 0 1 2.2E-03 0 0
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
1410 0 1 7.0E-04 0 0
CUI: C0003130
Disease: Anoxia
Anoxia
287 0 1 3.4E-03 0 0
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal
586 0 1 1.7E-03 0 0
CUI: C0750927
Disease: Apraxia, Developmental Verbal
Apraxia, Developmental Verbal
80 0 1 1.1E-02 0 0
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly
102 0 1 8.8E-03 0 0
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
2006 0 1 5.0E-04 0 0
CUI: C0003864
Disease: Arthritis
Arthritis
1072 0 1 9.2E-04 0 0
CUI: C0004096
Disease: Asthma
Asthma
2096 0 1 4.7E-04 0 0
CUI: C0004114
Disease: Astrocytoma
Astrocytoma
985 0 1 1.0E-03 0 0
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
2044 0 1 4.9E-04 0 0
CUI: C4703473
Disease: Atherosclerotic lesion
Atherosclerotic lesion
253 0 1 3.8E-03 0 0
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
939 0 1 1.1E-03 0 0
CUI: C1855642
Disease: Atrophy of alveolar ridges
Atrophy of alveolar ridges
3 0 1 7.1E-02 0 0
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
1071 0 1 9.2E-04 0 0
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
1758 0 1 5.7E-04 0 0
CUI: C1328843
Disease: Autoimmune vasculitis
Autoimmune vasculitis
7 0 1 5.6E-02 0 0
Autosomal dominant compelling helio ophthalmic outburst syndrome
26 0 1 2.7E-02 0 0