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: C0012833
Disease: Dizziness
Dizziness 		0 14 0 0 1 5.3E-02
CUI: C0085623
Disease: Akinesia
Akinesia 		0 3 0 0 1 0.12
CUI: C0220870
Disease: Lightheadedness
Lightheadedness 		0 1 0 0 1 0.17
CUI: C0221170
Disease: Muscular stiffness
Muscular stiffness 		0 6 0 0 1 9.1E-02
CUI: C0233689
Disease: Delusion of infidelity
Delusion of infidelity 		0 1 0 0 1 0.17
CUI: C0233763
Disease: Hallucinations, Visual
Hallucinations, Visual 		0 5 0 0 1 1.0E-01
CUI: C0234379
Disease: Resting Tremor
Resting Tremor 		0 5 0 0 1 1.0E-01
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
Autosomal Dominant Parkinsonism 		0 3 0 0 1 0.12
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		0 33 0 0 1 2.6E-02
CUI: C1847640
Disease: KUFOR-RAKEB SYNDROME
KUFOR-RAKEB SYNDROME 		0 16 0 0 1 4.8E-02
CUI: C1868675
Disease: PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE 		0 37 0 0 1 2.4E-02
CUI: C1963757
Disease: Dopamine dysregulation syndrome
Dopamine dysregulation syndrome 		0 1 0 0 1 0.17
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired 		0 12 0 0 1 5.9E-02
CUI: C4020732
Disease: Mitochondrial abnormalities
Mitochondrial abnormalities 		0 20 0 0 1 4.0E-02
CUI: C4274355
Disease: Autosomal dominant late onset Parkinson disease
Autosomal dominant late onset Parkinson disease 		0 5 0 0 1 1.0E-01
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		0 32 0 0 1 2.7E-02
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 1 1.1E-02 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 1 2.7E-02 0 0
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal 		109 0 1 7.2E-03 0 0
CUI: C0000846
Disease: Agenesis
Agenesis 		161 0 1 5.2E-03 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 2.4E-02 0 0
CUI: C0001363
Disease: Acute vascular insufficiency of intestine (disorder)
Acute vascular insufficiency of intestine (disorder) 		8 0 1 2.6E-02 0 0
CUI: C0001422
Disease: Adenofibroma
Adenofibroma 		8 0 1 2.6E-02 0 0
CUI: C0001429
Disease: Adenolymphoma
Adenolymphoma 		21 0 1 2.0E-02 0 0
CUI: C0001621
Disease: Adrenal Gland Diseases
Adrenal Gland Diseases 		9 0 1 2.6E-02 0 0