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: C4531121
Disease: Monotonic speech
Monotonic speech
9 0 7 0.44 0 0
CUI: C1836904
Disease: Spastic/hyperactive bladder
Spastic/hyperactive bladder
10 0 7 0.41 0 0
Orthostatic hypotension due to autonomic dysfunction
16 0 7 0.30 0 0
Parkinsonism with favorable response to dopaminergic medication
21 0 7 0.25 0 0
CUI: C0231688
Disease: Gait, Shuffling
Gait, Shuffling
28 0 8 0.24 0 0
Autosomal dominant late onset Parkinson disease
9 0 4 0.21 0 0
CUI: C0813217
Disease: Expressionless face
Expressionless face
31 0 7 0.18 0 0
CUI: C0401149
Disease: Chronic constipation
Chronic constipation
47 0 9 0.17 0 0
CUI: C0233763
Disease: Hallucinations, Visual
Hallucinations, Visual
39 0 7 0.15 0 0
CUI: C0085623
Disease: Akinesia
Akinesia
43 0 7 0.14 0 0
CUI: C1868596
Disease: Atypical Parkinson Disease
Atypical Parkinson Disease
11 0 3 0.14 0 0
CUI: C1269700
Disease: Caliectasis
Caliectasis
3 0 2 0.13 0 0
CUI: C1847363
Disease: Aplasia/Hypoplasia of the ribs
Aplasia/Hypoplasia of the ribs
3 0 2 0.13 0 0
Growth Deficiency and Mental Retardation with Facial Dysmorphism
4 0 2 0.12 0 0
CUI: C1846865
Disease: Substantia nigra gliosis
Substantia nigra gliosis
14 0 3 0.12 0 0
CUI: C0268250
Disease: Gaucher Disease, Type 2 (disorder)
Gaucher Disease, Type 2 (disorder)
6 0 2 0.11 0 0
CUI: C0234379
Disease: Resting Tremor
Resting Tremor
57 0 7 0.11 0 0
CUI: C4022873
Disease: Small pituitary gland
Small pituitary gland
7 0 2 0.11 0 0
CUI: C1843921
Disease: Postural instability
Postural instability
60 0 7 0.10 0 0
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired
60 0 7 0.10 0 0
CUI: C4551851
Disease: Cornelia de Lange Syndrome 1
Cornelia de Lange Syndrome 1
8 0 2 1.0E-01 0 0
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
Autosomal Dominant Parkinsonism
34 0 4 9.1E-02 0 0
CUI: C1851959
Disease: Fluctuations in consciousness
Fluctuations in consciousness
10 0 2 9.1E-02 0 0
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1
46 0 5 9.1E-02 0 0
CUI: C0271007
Disease: Phthisis bulbi
Phthisis bulbi
11 0 2 8.7E-02 0 0