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: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 1 7.5E-04 0 0
CUI: C1839603
Disease: Proximal tubulopathy
Proximal tubulopathy 		37 0 1 7.5E-04 0 0
CUI: C1849097
Disease: Loss of ability to walk
Loss of ability to walk 		37 0 1 7.5E-04 0 0
CUI: C1850599
Disease: Leigh Syndrome due to Mitochondrial Complex IV Deficiency
Leigh Syndrome due to Mitochondrial Complex IV Deficiency 		37 0 1 7.5E-04 0 0
CUI: C0035410
Disease: Rhabdomyolysis
Rhabdomyolysis 		36 0 1 7.5E-04 0 0
CUI: C1850597
Disease: Leigh Syndrome Due To Mitochondrial Complex II Deficiency
Leigh Syndrome Due To Mitochondrial Complex II Deficiency 		36 0 1 7.5E-04 0 0
CUI: C1850598
Disease: Leigh Syndrome due to Mitochondrial Complex III Deficiency
Leigh Syndrome due to Mitochondrial Complex III Deficiency 		36 0 1 7.5E-04 0 0
CUI: C1850600
Disease: Leigh Syndrome due to Mitochondrial Complex V Deficiency
Leigh Syndrome due to Mitochondrial Complex V Deficiency 		36 0 1 7.5E-04 0 0
CUI: C2931891
Disease: Necrotizing encephalopathy, infantile subacute, of Leigh
Necrotizing encephalopathy, infantile subacute, of Leigh 		36 0 1 7.5E-04 0 0
CUI: C1839888
Disease: Decreased activity of the pyruvate dehydrogenase complex
Decreased activity of the pyruvate dehydrogenase complex 		35 0 1 7.5E-04 0 0
CUI: C4021538
Disease: Mild neurosensory hearing impairment
Mild neurosensory hearing impairment 		35 0 1 7.5E-04 0 0
CUI: C0454651
Disease: Specific language impairment
Specific language impairment 		34 0 1 7.5E-04 0 0
CUI: C0878521
Disease: Beta thalassemia trait
Beta thalassemia trait 		34 0 1 7.5E-04 0 0
CUI: C4024923
Disease: Diffuse white matter abnormalities
Diffuse white matter abnormalities 		34 0 1 7.5E-04 0 0
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		33 9 1 7.5E-04 1 1.6E-03
CUI: C0031572
Disease: Phobia, Social
Phobia, Social 		33 0 1 7.5E-04 0 0
CUI: C1845251
Disease: Facial hypotonia
Facial hypotonia 		33 0 1 7.5E-04 0 0
CUI: C0026603
Disease: Motion Sickness
Motion Sickness 		32 0 1 7.5E-04 0 0
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery 		32 0 1 7.5E-04 0 0
CUI: C0742028
Disease: Cerebellar vermis atrophy
Cerebellar vermis atrophy 		32 0 1 7.5E-04 0 0
CUI: C1837066
Disease: Recurrent viral infection
Recurrent viral infection 		32 0 1 7.5E-04 0 0
CUI: C1298695
Disease: Hypoplasia of optic disc
Hypoplasia of optic disc 		31 0 1 7.5E-04 0 0
CUI: C1631597
Disease: VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) 		31 0 1 7.5E-04 0 0
CUI: C0751435
Disease: Hyperphenylalaninaemia
Hyperphenylalaninaemia 		30 0 1 7.5E-04 0 0
CUI: C1836508
Disease: Generalized tonic seizures
Generalized tonic seizures 		30 0 1 7.5E-04 0 0