Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Respiratory Distress Syndrome, Adult
434 0 1 1.7E-03 0 0
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
405 0 1 1.8E-03 0 0
Corpuscular Hemoglobin Concentration Mean
401 0 1 1.8E-03 0 0
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
336 0 1 2.0E-03 0 0
CUI: C0151449
Disease: Primary Sjögren's syndrome
Primary Sjögren's syndrome
312 0 1 2.2E-03 0 0
CUI: C0035126
Disease: Reperfusion Injury
Reperfusion Injury
300 0 1 2.2E-03 0 0
CUI: C0042384
Disease: Vasculitis
Vasculitis
294 0 1 2.2E-03 0 0
CUI: C0017668
Disease: Focal glomerulosclerosis
Focal glomerulosclerosis
281 0 1 2.3E-03 0 0
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
269 0 1 2.4E-03 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus
265 0 1 2.4E-03 0 0
Mucosa-Associated Lymphoid Tissue Lymphoma
264 0 1 2.4E-03 0 0
CUI: C1510472
Disease: Drug Dependence
Drug Dependence
248 0 1 2.5E-03 0 0
CUI: C0032227
Disease: Pleural effusion disorder
Pleural effusion disorder
227 0 1 2.6E-03 0 0
CUI: C0268731
Disease: Renal glomerular disease
Renal glomerular disease
221 0 1 2.7E-03 0 0
CUI: C0042029
Disease: Urinary tract infection
Urinary tract infection
219 0 1 2.7E-03 0 0
CUI: C0221056
Disease: Adult type dermatomyositis
Adult type dermatomyositis
218 0 1 2.7E-03 0 0
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
Pseudohyperkalemia Cardiff
218 0 1 2.7E-03 0 0
CUI: C1843013
Disease: Alzheimer disease, familial, type 3
Alzheimer disease, familial, type 3
213 0 1 2.7E-03 0 0
Multiple Sclerosis, Relapsing-Remitting
206 0 1 2.8E-03 0 0
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial
203 0 1 2.8E-03 0 0
CUI: C0003125
Disease: Anorexia Nervosa
Anorexia Nervosa
202 0 1 2.8E-03 0 0
CUI: C0035344
Disease: Retinopathy of Prematurity
Retinopathy of Prematurity
202 0 1 2.8E-03 0 0
CUI: C1658953
Disease: tumor vasculature
tumor vasculature
200 0 1 2.8E-03 0 0
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura
198 0 1 2.8E-03 0 0
CUI: C0699949
Disease: airway disease
airway disease
198 0 1 2.8E-03 0 0