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: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
Charcot-Marie-Tooth Disease, Type Ia (disorder) 		42 0 1 9.3E-04 0 0
CUI: C1853235
Disease: Sclerocornea
Sclerocornea 		42 0 1 9.3E-04 0 0
CUI: C0270834
Disease: Complex partial seizure with impairment of consciousness
Complex partial seizure with impairment of consciousness 		41 10 1 9.3E-04 1 9.6E-03
CUI: C0858600
Disease: Taste sweet
Taste sweet 		41 0 1 9.3E-04 0 0
CUI: C0877165
Disease: Short phalanx of finger
Short phalanx of finger 		41 0 1 9.3E-04 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 1 9.3E-04 0 0
CUI: C4021741
Disease: Abnormal cortical bone morphology
Abnormal cortical bone morphology 		41 0 1 9.3E-04 0 0
CUI: C0085606
Disease: Urgency of micturition
Urgency of micturition 		40 0 1 9.3E-04 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		40 0 1 9.3E-04 0 0
CUI: C1838951
Disease: LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY 		40 0 1 9.3E-04 0 0
CUI: C0085615
Disease: Right bundle branch block
Right bundle branch block 		39 0 1 9.3E-04 0 0
CUI: C1844548
Disease: Hypoplastic finger
Hypoplastic finger 		39 0 1 9.3E-04 0 0
CUI: C1847515
Disease: Paroxysmal involuntary eye movements
Paroxysmal involuntary eye movements 		39 0 1 9.3E-04 0 0
CUI: C4021546
Disease: Abnormal mitochondria in muscle tissue
Abnormal mitochondria in muscle tissue 		39 0 1 9.3E-04 0 0
CUI: C0158683
Disease: Polycystic liver disease
Polycystic liver disease 		38 0 1 9.3E-04 0 0
CUI: C0239399
Disease: Short extremities
Short extremities 		38 0 1 9.3E-04 0 0
CUI: C1846647
Disease: DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE (disorder) 		38 0 1 9.3E-04 0 0
CUI: C0239594
Disease: Short finger
Short finger 		37 0 1 9.4E-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 9.4E-04 0 0
CUI: C0018810
Disease: heart rate
heart rate 		36 0 1 9.4E-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 9.4E-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 9.4E-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 9.4E-04 0 0
CUI: C2931891
Disease: Necrotizing encephalopathy, infantile subacute, of Leigh
Necrotizing encephalopathy, infantile subacute, of Leigh 		36 0 1 9.4E-04 0 0
CUI: C0078982
Disease: Arhinencephaly
Arhinencephaly 		35 0 1 9.4E-04 0 0