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: C3665346
Disease: Unspecified visual loss
Unspecified visual loss 		235 0 13 4.8E-02 0 0
CUI: C4020732
Disease: Mitochondrial abnormalities
Mitochondrial abnormalities 		83 0 6 4.7E-02 0 0
CUI: C0026706
Disease: Mucopolysaccharidosis III
Mucopolysaccharidosis III 		17 0 3 4.6E-02 0 0
CUI: C0338460
Disease: Argyrophilic grain disease
Argyrophilic grain disease 		18 0 3 4.5E-02 0 0
CUI: C0751071
Disease: Familial Dementia
Familial Dementia 		18 0 3 4.5E-02 0 0
CUI: C0949856
Disease: Oxidative Phosphorylation Deficiencies
Oxidative Phosphorylation Deficiencies 		18 0 3 4.5E-02 0 0
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies 		44 0 4 4.4E-02 0 0
CUI: C0262405
Disease: Cerebral dysfunction
Cerebral dysfunction 		45 0 4 4.3E-02 0 0
CUI: C0751706
Disease: Primary Progressive Nonfluent Aphasia
Primary Progressive Nonfluent Aphasia 		21 0 3 4.3E-02 0 0
CUI: C1846868
Disease: Parkinsonism with favorable response to dopaminergic medication
Parkinsonism with favorable response to dopaminergic medication 		21 0 3 4.3E-02 0 0
CUI: C1868773
Disease: Diabetic encephalopathy
Diabetic encephalopathy 		21 0 3 4.3E-02 0 0
CUI: C0017205
Disease: Gaucher Disease
Gaucher Disease 		143 0 8 4.3E-02 0 0
CUI: C0003635
Disease: Apraxias
Apraxias 		71 0 5 4.3E-02 0 0
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
Frontotemporal Lobar Degeneration 		195 0 10 4.2E-02 0 0
CUI: C4285807
Disease: Behavioral and psychological symptoms of dementia
Behavioral and psychological symptoms of dementia 		72 0 5 4.2E-02 0 0
CUI: C1865412
Disease: Abnormal lower motor neuron morphology
Abnormal lower motor neuron morphology 		23 0 3 4.2E-02 0 0
CUI: C3887612
Disease: Psychomotor Agitation
Psychomotor Agitation 		26 0 3 4.1E-02 0 0
CUI: C0231688
Disease: Gait, Shuffling
Gait, Shuffling 		28 0 3 3.9E-02 0 0
CUI: C0242423
Disease: Ramsay Hunt Paralysis Syndrome
Ramsay Hunt Paralysis Syndrome 		28 0 3 3.9E-02 0 0
CUI: C0752097
Disease: Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Juvenile Parkinson Disease 		28 0 3 3.9E-02 0 0
CUI: C0752101
Disease: Parkinsonism, Experimental
Parkinsonism, Experimental 		28 0 3 3.9E-02 0 0
CUI: C0752104
Disease: Familial Juvenile Parkinsonism
Familial Juvenile Parkinsonism 		28 0 3 3.9E-02 0 0
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		373 0 16 3.9E-02 0 0
CUI: C1836791
Disease: Tortuous cerebral arteries
Tortuous cerebral arteries 		2 0 2 3.9E-02 0 0
CUI: C1853507
Disease: Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations
Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations 		2 0 2 3.9E-02 0 0