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: C0679407
Disease: Gastrointestinal dysfunction
Gastrointestinal dysfunction 		16 0 4 0.12 0 0
CUI: C4274355
Disease: Autosomal dominant late onset Parkinson disease
Autosomal dominant late onset Parkinson disease 		9 0 3 0.12 0 0
CUI: C0338455
Disease: Dementia of frontal lobe type
Dementia of frontal lobe type 		20 0 4 0.11 0 0
CUI: C1868596
Disease: Atypical Parkinson Disease
Atypical Parkinson Disease 		11 0 3 0.11 0 0
CUI: C0278097
Disease: Abnormal male sexual function
Abnormal male sexual function 		12 0 3 0.10 0 0
CUI: C1112443
Disease: Male sexual dysfunction
Male sexual dysfunction 		12 0 3 0.10 0 0
CUI: C3888102
Disease: Frontotemporal Dementia With Motor Neuron Disease
Frontotemporal Dementia With Motor Neuron Disease 		13 0 3 1.0E-01 0 0
CUI: C4020732
Disease: Mitochondrial abnormalities
Mitochondrial abnormalities 		83 20 9 9.6E-02 1 4.0E-02
CUI: C0270726
Disease: Alexander Disease
Alexander Disease 		27 0 4 9.3E-02 0 0
CUI: C1395088
Disease: Nervous system--Degeneration
Nervous system--Degeneration 		4 0 2 9.1E-02 0 0
CUI: C1853445
Disease: PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET
PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET 		4 0 2 9.1E-02 0 0
CUI: C2931072
Disease: Epidermolysa bullosa simplex and limb girdle muscular dystrophy
Epidermolysa bullosa simplex and limb girdle muscular dystrophy 		4 0 2 9.1E-02 0 0
CUI: C3825276
Disease: Stereotyped behavior (Psychiatry)
Stereotyped behavior (Psychiatry) 		5 0 2 8.7E-02 0 0
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1 		46 0 5 8.2E-02 0 0
CUI: C1112442
Disease: Female sexual dysfunction
Female sexual dysfunction 		22 0 3 7.7E-02 0 0
CUI: C1135188
Disease: Critical illness myopathy
Critical illness myopathy 		8 0 2 7.7E-02 0 0
CUI: C1853833
Disease: Parkinson Disease 6, Autosomal Recessive Early-Onset
Parkinson Disease 6, Autosomal Recessive Early-Onset 		9 0 2 7.4E-02 0 0
CUI: C2718001
Disease: Protein Misfolding Disorders
Protein Misfolding Disorders 		38 0 4 7.4E-02 0 0
CUI: C4531121
Disease: Monotonic speech
Monotonic speech 		9 0 2 7.4E-02 0 0
CUI: C1836904
Disease: Spastic/hyperactive bladder
Spastic/hyperactive bladder 		10 0 2 7.1E-02 0 0
CUI: C0522055
Disease: Electrocardiogram abnormal
Electrocardiogram abnormal 		11 0 2 6.9E-02 0 0
CUI: C1847640
Disease: KUFOR-RAKEB SYNDROME
KUFOR-RAKEB SYNDROME 		11 0 2 6.9E-02 0 0
CUI: C4721541
Disease: PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) 		11 0 2 6.9E-02 0 0
CUI: C0085623
Disease: Akinesia
Akinesia 		43 0 4 6.8E-02 0 0
CUI: C0231688
Disease: Gait, Shuffling
Gait, Shuffling 		28 0 3 6.7E-02 0 0