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 4.3E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 9.4E-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 6.7E-02 0 0
Abnormal mitochondria in muscle tissue
39 0 1 2.4E-02 0 0
Abnormal morphology of the cerebellar cortex
2 0 2 0.50 0 0
CUI: C0035300
Disease: Abnormal retinal morphology
Abnormal retinal morphology
13 0 1 6.2E-02 0 0
Abnormal thalamic MRI signal intensity
4 0 2 0.33 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
115 0 1 8.5E-03 0 0
CUI: C0522214
Disease: Abnormal visual evoked potential
Abnormal visual evoked potential
55 0 1 1.7E-02 0 0
Abnormality of central motor conduction
1 0 1 0.25 0 0
Abnormality of the autonomic nervous system
3 0 1 0.17 0 0
Abnormality of the cerebrospinal fluid
3 0 1 0.17 0 0
Abnormality of the extraocular muscles
4 0 1 0.14 0 0
CUI: C4023042
Disease: Abnormality of the mitochondrion
Abnormality of the mitochondrion
10 0 2 0.17 0 0
CUI: C4025751
Disease: Abnormality of the pancreas
Abnormality of the pancreas
13 0 1 6.2E-02 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
205 0 1 4.8E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 2 9.9E-03 0 0
CUI: C1321756
Disease: Achalasia
Achalasia
40 0 2 4.8E-02 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic
209 0 1 4.7E-03 0 0
CUI: C0234376
Disease: Action Tremor
Action Tremor
95 0 1 1.0E-02 0 0
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
656 0 1 1.5E-03 0 0
CUI: C0220624
Disease: Adult Brain Neoplasm
Adult Brain Neoplasm
15 0 1 5.6E-02 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause
129 0 1 7.6E-03 0 0