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: C0085623
Disease: Akinesia
Akinesia
43 0 1 2.1E-02 0 0
CUI: C0860659
Disease: Aloof
Aloof
81 0 1 1.2E-02 0 0
CUI: C0338488
Disease: Alternating hemiplegia of childhood
Alternating hemiplegia of childhood
8 0 1 8.3E-02 0 0
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
1114 0 1 8.9E-04 0 0
CUI: C1563715
Disease: Andersen Syndrome
Andersen Syndrome
23 0 1 3.7E-02 0 0
CUI: C0002886
Disease: Anemia, Macrocytic
Anemia, Macrocytic
51 2 1 1.8E-02 1 0.33
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell
434 0 1 2.3E-03 0 0
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate
139 0 1 7.0E-03 0 0
CUI: C0003467
Disease: Anxiety
Anxiety
1048 0 1 9.5E-04 0 0
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders
840 0 1 1.2E-03 0 0
CUI: C1856694
Disease: Areflexia of lower limbs
Areflexia of lower limbs
24 0 1 3.6E-02 0 0
Arrhythmogenic Right Ventricular Dysplasia
82 0 1 1.2E-02 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis
198 0 1 5.0E-03 0 0
CUI: C0004045
Disease: Asphyxia Neonatorum
Asphyxia Neonatorum
45 0 1 2.0E-02 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 68 2 2.3E-03 1 1.4E-02
Atrophy/Degeneration affecting the cerebrum
1 1 1 0.20 1 0.50
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
1112 0 1 9.0E-04 0 0
Autosomal Dominant Myotubular Myopathy
13 0 1 5.9E-02 0 0
Autosomal dominant retinitis pigmentosa
85 0 1 1.1E-02 0 0
Autosomal Recessive Centronuclear Myopathy
16 0 1 5.0E-02 0 0
AV Block Second Degree by ECG Finding
4 0 1 0.12 0 0
CUI: C1843697
Disease: Axial muscle weakness
Axial muscle weakness
28 0 1 3.1E-02 0 0
CUI: C3267178
Disease: Axial myopathy
Axial myopathy
3 0 1 0.14 0 0
CUI: C1837496
Disease: Axonal degeneration
Axonal degeneration
17 0 1 4.8E-02 0 0
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex
218 11 2 9.0E-03 1 8.3E-02