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: C0239548
Disease: Fasciculation, Tongue
Fasciculation, Tongue 		21 7 4 6.2E-02 1 4.3E-02
CUI: C0333641
Disease: Atrophic
Atrophic 		58 0 6 6.0E-02 0 0
CUI: C0917808
Disease: Vegetative State
Vegetative State 		5 0 3 6.0E-02 0 0
CUI: C1859569
Disease: BARDET-BIEDL SYNDROME 11
BARDET-BIEDL SYNDROME 11 		5 0 3 6.0E-02 0 0
CUI: C0270834
Disease: Complex partial seizure with impairment of consciousness
Complex partial seizure with impairment of consciousness 		41 0 5 6.0E-02 0 0
CUI: C0751354
Disease: Myoclonus, Action
Myoclonus, Action 		6 1 3 5.9E-02 1 5.9E-02
CUI: C0393547
Disease: Bulbospinal Neuronopathy
Bulbospinal Neuronopathy 		7 0 3 5.8E-02 0 0
CUI: C0524582
Disease: Mulibrey Nanism
Mulibrey Nanism 		7 0 3 5.8E-02 0 0
CUI: C0795858
Disease: Chromosome 15q, trisomy
Chromosome 15q, trisomy 		7 0 3 5.8E-02 0 0
CUI: C0271390
Disease: Nystagmus, End-Position
Nystagmus, End-Position 		26 0 4 5.7E-02 0 0
CUI: C1859305
Disease: Cerebellar Ataxia and Hypogonadotropic Hypogonadism
Cerebellar Ataxia and Hypogonadotropic Hypogonadism 		8 0 3 5.7E-02 0 0
CUI: C2608055
Disease: Hereditary Renal Cell Carcinoma
Hereditary Renal Cell Carcinoma 		8 0 3 5.7E-02 0 0
CUI: C4024957
Disease: Proximal spinal muscular atrophy
Proximal spinal muscular atrophy 		10 0 3 5.5E-02 0 0
CUI: C4021757
Disease: EEG with polyspike wave complexes
EEG with polyspike wave complexes 		30 0 4 5.4E-02 0 0
CUI: C4302185
Disease: Atypical Parkinsonism
Atypical Parkinsonism 		30 0 4 5.4E-02 0 0
CUI: C1847164
Disease: Morning myoclonic jerks
Morning myoclonic jerks 		11 0 3 5.4E-02 0 0
CUI: C1856565
Disease: Progressive psychomotor deterioration
Progressive psychomotor deterioration 		11 0 3 5.4E-02 0 0
CUI: C3661519
Disease: Hereditary Motor Neuronopathy
Hereditary Motor Neuronopathy 		12 0 3 5.3E-02 0 0
CUI: C4280747
Disease: Choking episodes
Choking episodes 		12 1 3 5.3E-02 1 5.9E-02
CUI: C1801950
Disease: Opitz-G syndrome, type 2
Opitz-G syndrome, type 2 		13 0 3 5.2E-02 0 0
CUI: C1841984
Disease: GLOMUVENOUS MALFORMATIONS
GLOMUVENOUS MALFORMATIONS 		13 0 3 5.2E-02 0 0
CUI: C0699743
Disease: Congenital muscular dystrophy (disorder)
Congenital muscular dystrophy (disorder) 		54 0 5 5.2E-02 0 0
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
Peripheral demyelinating neuropathy 		95 0 7 5.1E-02 0 0
CUI: C0012569
Disease: Diplopia
Diplopia 		75 0 6 5.1E-02 0 0
CUI: C3698239
Disease: Cerebral cortex myoclonus
Cerebral cortex myoclonus 		14 0 3 5.1E-02 0 0