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: C0878575
Disease: Peripheral demyelination
Peripheral demyelination 		27 0 8 0.11 0 0
CUI: C0240735
Disease: Personality Change
Personality Change 		43 0 9 0.10 0 0
CUI: C0014059
Disease: Encephalomyelitis, Acute Disseminated
Encephalomyelitis, Acute Disseminated 		24 0 7 0.10 0 0
CUI: C1858995
Disease: Decreased circulating progesterone
Decreased circulating progesterone 		5 0 5 9.6E-02 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy 		190 0 21 9.5E-02 0 0
CUI: C4025319
Disease: Cessation of head growth
Cessation of head growth 		6 0 5 9.4E-02 0 0
CUI: C1847967
Disease: OVARIOLEUKODYSTROPHY
OVARIOLEUKODYSTROPHY 		7 0 5 9.3E-02 0 0
CUI: C0751267
Disease: Encephalopathy, Subacute Necrotizing, Infantile
Encephalopathy, Subacute Necrotizing, Infantile 		9 0 5 8.9E-02 0 0
CUI: C0751268
Disease: Encephalopathy, Subacute Necrotizing, Juvenile
Encephalopathy, Subacute Necrotizing, Juvenile 		9 0 5 8.9E-02 0 0
CUI: C0017639
Disease: Gliosis
Gliosis 		102 0 12 8.5E-02 0 0
CUI: C0393847
Disease: Multifocal motor neuropathy
Multifocal motor neuropathy 		13 0 5 8.3E-02 0 0
CUI: C0029134
Disease: Optic Neuritis
Optic Neuritis 		79 0 10 8.3E-02 0 0
CUI: C2960129
Disease: Vanishing white matter disease
Vanishing white matter disease 		14 0 5 8.2E-02 0 0
CUI: C2677328
Disease: Cerebral hypomyelination
Cerebral hypomyelination 		29 0 6 8.0E-02 0 0
CUI: C0011253
Disease: Delusions
Delusions 		62 0 8 7.5E-02 0 0
CUI: C1837388
Disease: Abnormal pattern of respiration
Abnormal pattern of respiration 		20 0 5 7.5E-02 0 0
CUI: C1859014
Disease: Primary gonadal insufficiency
Primary gonadal insufficiency 		21 0 5 7.4E-02 0 0
CUI: C1850597
Disease: Leigh Syndrome Due To Mitochondrial Complex II Deficiency
Leigh Syndrome Due To Mitochondrial Complex II Deficiency 		36 0 6 7.3E-02 0 0
CUI: C1850598
Disease: Leigh Syndrome due to Mitochondrial Complex III Deficiency
Leigh Syndrome due to Mitochondrial Complex III Deficiency 		36 0 6 7.3E-02 0 0
CUI: C1850600
Disease: Leigh Syndrome due to Mitochondrial Complex V Deficiency
Leigh Syndrome due to Mitochondrial Complex V Deficiency 		36 0 6 7.3E-02 0 0
CUI: C2931891
Disease: Necrotizing encephalopathy, infantile subacute, of Leigh
Necrotizing encephalopathy, infantile subacute, of Leigh 		36 0 6 7.3E-02 0 0
CUI: C1850599
Disease: Leigh Syndrome due to Mitochondrial Complex IV Deficiency
Leigh Syndrome due to Mitochondrial Complex IV Deficiency 		37 0 6 7.2E-02 0 0
CUI: C0011303
Disease: Demyelinating Diseases
Demyelinating Diseases 		156 0 14 7.2E-02 0 0
CUI: C0393819
Disease: Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating 		82 0 9 7.2E-02 0 0
CUI: C4324721
Disease: Radiologically isolated syndrome
Radiologically isolated syndrome 		8 0 4 7.1E-02 0 0