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: C0268243
Disease: Niemann-Pick Disease, Type B
Niemann-Pick Disease, Type B
0 57 0 0 1 5.7E-03
CUI: C1336970
Disease: Visual Manifestations
Visual Manifestations
0 1 0 0 1 8.3E-03
NIEMANN-PICK DISEASE, INTERMEDIATE, PROTRACTED NEUROVISCERAL (disorder)
0 2 0 0 1 8.3E-03
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced
5 0 1 2.2E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic
11 0 1 2.2E-03 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis
1 0 1 2.3E-03 0 0
CUI: C0001344
Disease: Acute pharyngitis
Acute pharyngitis
9 0 1 2.2E-03 0 0
CUI: C0001433
Disease: Adenoma, Acidophil
Adenoma, Acidophil
2 0 1 2.3E-03 0 0
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders
9 0 1 2.2E-03 0 0
CUI: C0001614
Disease: Adrenal Cortex Diseases
Adrenal Cortex Diseases
13 0 1 2.2E-03 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases
9 0 1 2.2E-03 0 0
CUI: C0001723
Disease: Affective Disorders, Psychotic
Affective Disorders, Psychotic
17 0 1 2.2E-03 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis
55 0 1 2.0E-03 0 0
CUI: C0001825
Disease: Agraphia
Agraphia
3 0 1 2.3E-03 0 0
CUI: C0001889
Disease: Akinetic Mutism
Akinetic Mutism
1 0 1 2.3E-03 0 0
CUI: C0001957
Disease: Alcohol Withdrawal Delirium
Alcohol Withdrawal Delirium
23 0 1 2.2E-03 0 0
CUI: C0002020
Disease: Alexithymia
Alexithymia
39 0 1 2.1E-03 0 0
CUI: C0002063
Disease: Alkalosis
Alkalosis
25 0 1 2.2E-03 0 0
CUI: C0002103
Disease: Atopic rhinitis
Atopic rhinitis
13 0 1 2.2E-03 0 0
CUI: C0002351
Disease: Altitude Sickness
Altitude Sickness
10 0 1 2.2E-03 0 0
Amino Acid Metabolism, Inborn Errors
20 0 1 2.2E-03 0 0
CUI: C0002690
Disease: Amputation Stumps
Amputation Stumps
11 0 1 2.2E-03 0 0
CUI: C0002876
Disease: Congenital dyserythropoietic anemia
Congenital dyserythropoietic anemia
24 0 1 2.2E-03 0 0
CUI: C0002881
Disease: Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital
27 0 1 2.1E-03 0 0
CUI: C0002884
Disease: Hypochromic anemia
Hypochromic anemia
16 0 1 2.2E-03 0 0