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: 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: C1836852
Disease: Curvilinear intracellular accumulation of autofluorescent lipopigment storage material
Curvilinear intracellular accumulation of autofluorescent lipopigment storage material 		6 0 2 0.20 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
CUI: C1850100
Disease: PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder)
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
CUI: C1843792
Disease: FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED 		8 0 1 7.7E-02 0 0
CUI: C4025728
Disease: Increased neuronal autofluorescent lipopigment
Increased neuronal autofluorescent lipopigment 		8 0 2 0.17 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
CUI: C1853833
Disease: Parkinson Disease 6, Autosomal Recessive Early-Onset
Parkinson Disease 6, Autosomal Recessive Early-Onset 		9 0 1 7.1E-02 0 0
CUI: C1866282
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 6
CEROID LIPOFUSCINOSIS, NEURONAL, 6 		9 0 3 0.25 0 0
CUI: C4274355
Disease: Autosomal dominant late onset Parkinson disease
Autosomal dominant late onset Parkinson disease 		9 0 1 7.1E-02 0 0
CUI: C4531121
Disease: Monotonic speech
Monotonic speech 		9 0 1 7.1E-02 0 0
CUI: C0338457
Disease: Aphasia, Progressive
Aphasia, Progressive 		10 0 1 6.7E-02 0 0
CUI: C1836904
Disease: Spastic/hyperactive bladder
Spastic/hyperactive bladder 		10 0 1 6.7E-02 0 0
CUI: C1851959
Disease: Fluctuations in consciousness
Fluctuations in consciousness 		10 0 1 6.7E-02 0 0
CUI: C4524839
Disease: Recurrent Head and Neck Squamous Cell Carcinoma
Recurrent Head and Neck Squamous Cell Carcinoma 		10 0 1 6.7E-02 0 0