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: C0270715
Disease: Degenerative Diseases, Central Nervous System
Degenerative Diseases, Central Nervous System 		43 0 40 0.93 0 0
CUI: C0751071
Disease: Familial Dementia
Familial Dementia 		18 0 5 9.4E-02 0 0
CUI: C0349081
Disease: Dementia in Parkinson's disease
Dementia in Parkinson's disease 		9 0 4 8.9E-02 0 0
CUI: C0149875
Disease: Primary dysmenorrhea
Primary dysmenorrhea 		13 0 4 8.2E-02 0 0
CUI: C0242423
Disease: Ramsay Hunt Paralysis Syndrome
Ramsay Hunt Paralysis Syndrome 		28 0 5 7.9E-02 0 0
CUI: C0752097
Disease: Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Juvenile Parkinson Disease 		28 0 5 7.9E-02 0 0
CUI: C0752101
Disease: Parkinsonism, Experimental
Parkinsonism, Experimental 		28 0 5 7.9E-02 0 0
CUI: C0752104
Disease: Familial Juvenile Parkinsonism
Familial Juvenile Parkinsonism 		28 0 5 7.9E-02 0 0
CUI: C0751262
Disease: Adult Learning Disorders
Adult Learning Disorders 		29 0 5 7.8E-02 0 0
CUI: C0751263
Disease: Learning Disturbance
Learning Disturbance 		29 0 5 7.8E-02 0 0
CUI: C1330966
Disease: Developmental Academic Disorder
Developmental Academic Disorder 		29 0 5 7.8E-02 0 0
CUI: C0011263
Disease: Multi-infarct dementia
Multi-infarct dementia 		30 0 5 7.7E-02 0 0
CUI: C0273115
Disease: Lung Injury
Lung Injury 		30 0 5 7.7E-02 0 0
CUI: C0338460
Disease: Argyrophilic grain disease
Argyrophilic grain disease 		18 0 4 7.4E-02 0 0
CUI: C0752100
Disease: Autosomal Recessive Parkinsonism
Autosomal Recessive Parkinsonism 		33 0 5 7.4E-02 0 0
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
Autosomal Dominant Parkinsonism 		34 0 5 7.2E-02 0 0
CUI: C0751706
Disease: Primary Progressive Nonfluent Aphasia
Primary Progressive Nonfluent Aphasia 		21 0 4 7.0E-02 0 0
CUI: C1868773
Disease: Diabetic encephalopathy
Diabetic encephalopathy 		21 0 4 7.0E-02 0 0
CUI: C1868675
Disease: PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE 		67 0 7 7.0E-02 0 0
CUI: C1858680
Disease: Familial encephalopathy with neuroserpin inclusion bodies
Familial encephalopathy with neuroserpin inclusion bodies 		7 0 3 6.8E-02 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition 		23 0 4 6.8E-02 0 0
CUI: C0006635
Disease: Cadmium poisoning
Cadmium poisoning 		8 0 3 6.7E-02 0 0
CUI: C0752105
Disease: Parkinsonism, Juvenile
Parkinsonism, Juvenile 		40 0 5 6.7E-02 0 0
CUI: C2931784
Disease: Amyloid angiopathy
Amyloid angiopathy 		9 0 3 6.5E-02 0 0
CUI: C0525041
Disease: Neurobehavioral Manifestations
Neurobehavioral Manifestations 		77 0 7 6.4E-02 0 0