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: C3696376
Disease: 3-Methylglutaconic Aciduria
3-Methylglutaconic Aciduria
20 0 1 5.0E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 9.7E-03 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.3E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 1 1.1E-03 0 0
CUI: C4476793
Disease: Abnormal cell morphology
Abnormal cell morphology
12 0 1 8.3E-02 0 0
Abnormal morphology of the cerebellar cortex
2 0 1 0.50 0 0
CUI: C0035300
Disease: Abnormal retinal morphology
Abnormal retinal morphology
13 0 1 7.7E-02 0 0
Abnormal thalamic MRI signal intensity
4 0 1 0.25 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
115 0 1 8.7E-03 0 0
CUI: C0522214
Disease: Abnormal visual evoked potential
Abnormal visual evoked potential
55 0 1 1.8E-02 0 0
Abnormality of central motor conduction
1 0 1 1.00 0 0
Abnormality of the cerebrospinal fluid
3 0 1 0.33 0 0
Abnormality of the extraocular muscles
4 0 1 0.25 0 0
CUI: C4023042
Disease: Abnormality of the mitochondrion
Abnormality of the mitochondrion
10 0 1 1.0E-01 0 0
CUI: C4025751
Disease: Abnormality of the pancreas
Abnormality of the pancreas
13 0 1 7.7E-02 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
205 0 1 4.9E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 5.0E-03 0 0
CUI: C1321756
Disease: Achalasia
Achalasia
40 0 1 2.5E-02 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic
209 0 1 4.8E-03 0 0
CUI: C0234376
Disease: Action Tremor
Action Tremor
95 0 1 1.1E-02 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause
129 0 1 7.8E-03 0 0
CUI: C0085623
Disease: Akinesia
Akinesia
43 0 1 2.3E-02 0 0
CUI: C0205710
Disease: Alpers Syndrome (disorder)
Alpers Syndrome (disorder)
28 128 1 3.6E-02 15 0.11
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
3397 0 1 2.9E-04 0 0
CUI: C0002871
Disease: Anemia
Anemia
847 0 1 1.2E-03 0 0