Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Lewy Body Variant of Alzheimer Disease
4 0 1 0.11 0 0
PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET
4 0 1 0.11 0 0
CUI: C1866284
Disease: Motor deterioration
Motor deterioration
14 0 2 0.11 0 0
CUI: C4477086
Disease: Cotton wool plaques
Cotton wool plaques
4 0 1 0.11 0 0
Ceroid Lipofuscinosis, Neuronal, Parry Type
5 0 1 1.0E-01 0 0
CUI: C1969363
Disease: Middle age onset
Middle age onset
5 0 1 1.0E-01 0 0
CUI: C0042790
Disease: Vision Disorders
Vision Disorders
6 0 1 9.1E-02 0 0
CUI: C0233769
Disease: Micropsia
Micropsia
6 0 1 9.1E-02 0 0
CUI: C0233771
Disease: Macropsia
Macropsia
6 0 1 9.1E-02 0 0
CUI: C0268250
Disease: Gaucher Disease, Type 2 (disorder)
Gaucher Disease, Type 2 (disorder)
6 0 1 9.1E-02 0 0
CUI: C1876161
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 2
CEROID LIPOFUSCINOSIS, NEURONAL, 2
6 0 1 9.1E-02 0 0
CUI: C3489704
Disease: Vision Disability
Vision Disability
6 0 1 9.1E-02 0 0
CUI: C0030508
Disease: Parasomnia
Parasomnia
7 0 1 8.3E-02 0 0
CUI: C0270733
Disease: Striatonigral Degeneration
Striatonigral Degeneration
7 0 1 8.3E-02 0 0
CUI: C0338473
Disease: Neuroaxonal Dystrophies
Neuroaxonal Dystrophies
7 0 1 8.3E-02 0 0
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder)
7 0 1 8.3E-02 0 0
CUI: C0026613
Disease: Motor Skills Disorders
Motor Skills Disorders
8 0 1 7.7E-02 0 0
CUI: C0037019
Disease: Shy-Drager Syndrome
Shy-Drager Syndrome
8 0 1 7.7E-02 0 0
CUI: C0729555
Disease: Infection of digestive system
Infection of digestive system
8 0 1 7.7E-02 0 0
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
8 0 1 7.7E-02 0 0
Juvenile Neuronal Ceroid Lipofuscinosis
52 0 4 7.4E-02 0 0
CUI: C0349081
Disease: Dementia in Parkinson's disease
Dementia in Parkinson's disease
9 0 1 7.1E-02 0 0
CUI: C0748903
Disease: spinal cord involvement
spinal cord involvement
9 0 1 7.1E-02 0 0
Parkinson Disease 6, Autosomal Recessive Early-Onset
9 0 1 7.1E-02 0 0
Autosomal dominant late onset Parkinson disease
9 0 1 7.1E-02 0 0