Source: ALL
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: C0410740
Disease: Acquired deformity of finger
Acquired deformity of finger 		5 0 1 0.11 0 0
CUI: C0750194
Disease: Non-sustained ventricular tachycardia
Non-sustained ventricular tachycardia 		5 0 1 0.11 0 0
CUI: C1393871
Disease: Congenital finger flexion contractures
Congenital finger flexion contractures 		5 0 1 0.11 0 0
CUI: C1850293
Disease: Severe platyspondyly
Severe platyspondyly 		5 0 1 0.11 0 0
CUI: C1851313
Disease: Limited shoulder movement
Limited shoulder movement 		5 0 1 0.11 0 0
CUI: C1855350
Disease: Inferior vermis hypoplasia
Inferior vermis hypoplasia 		5 0 1 0.11 0 0
CUI: C1862481
Disease: Limited wrist extension
Limited wrist extension 		5 0 1 0.11 0 0
CUI: C3808039
Disease: Nemaline bodies
Nemaline bodies 		15 0 2 0.11 0 0
CUI: C4025763
Disease: Abnormality of the rib cage
Abnormality of the rib cage 		16 0 2 0.11 0 0
CUI: C0175778
Disease: Larsen syndrome
Larsen syndrome 		6 0 1 1.0E-01 0 0
CUI: C0265642
Disease: Talipes Equinovalgus
Talipes Equinovalgus 		6 0 1 1.0E-01 0 0
CUI: C0340517
Disease: Atrial thrombosis
Atrial thrombosis 		6 0 1 1.0E-01 0 0
CUI: C0752143
Disease: Intracranial Thrombosis
Intracranial Thrombosis 		6 0 1 1.0E-01 0 0
CUI: C1832598
Disease: Narrow vertebral interpedicular distance
Narrow vertebral interpedicular distance 		6 0 1 1.0E-01 0 0
CUI: C1852085
Disease: Digitotalar Dysmorphism
Digitotalar Dysmorphism 		6 0 1 1.0E-01 0 0
CUI: C1857483
Disease: Decreased palmar creases
Decreased palmar creases 		6 0 1 1.0E-01 0 0
CUI: C1861349
Disease: Absent distal interphalangeal creases
Absent distal interphalangeal creases 		6 0 1 1.0E-01 0 0
CUI: C4025571
Disease: Type 1 fibers relatively smaller than type 2 fibers
Type 1 fibers relatively smaller than type 2 fibers 		6 0 1 1.0E-01 0 0
CUI: C4025712
Disease: Abnormality of the cerebellar vermis
Abnormality of the cerebellar vermis 		6 0 1 1.0E-01 0 0
CUI: C0410653
Disease: Atlantoaxial instability
Atlantoaxial instability 		7 0 1 9.1E-02 0 0
CUI: C0546125
Disease: Nemaline Myopathy, Childhood Onset
Nemaline Myopathy, Childhood Onset 		7 0 1 9.1E-02 0 0
CUI: C1842160
Disease: MYOPATHY, MYOSIN STORAGE (disorder)
MYOPATHY, MYOSIN STORAGE (disorder) 		7 0 1 9.1E-02 0 0
CUI: C1859111
Disease: Enlarged joints
Enlarged joints 		7 0 1 9.1E-02 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 8.3E-02 0 0
CUI: C0007177
Disease: Cardiac Tamponade
Cardiac Tamponade 		8 0 1 8.3E-02 0 0