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: C0236701
Disease: Cocaine-induced mood disorder
Cocaine-induced mood disorder 		1 0 1 1.00 0 0
CUI: C4747991
Disease: PARKINSONISM-DYSTONIA, INFANTILE, 2
PARKINSONISM-DYSTONIA, INFANTILE, 2 		1 0 1 1.00 0 0
CUI: C0241657
Disease: Abnormality of the vasculature
Abnormality of the vasculature 		4 0 1 0.25 0 0
CUI: C4476759
Disease: Stooped posture
Stooped posture 		6 0 1 0.17 0 0
CUI: C1850100
Disease: PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder)
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder) 		7 0 1 0.14 0 0
CUI: C0860609
Disease: Inappropriate crying
Inappropriate crying 		8 0 1 0.12 0 0
CUI: C0085637
Disease: Oculogyric crisis
Oculogyric crisis 		9 0 1 0.11 0 0
CUI: C0743072
Disease: Depression, psychotic
Depression, psychotic 		11 0 1 9.1E-02 0 0
CUI: C3272399
Disease: Gastric Neuroendocrine Tumor
Gastric Neuroendocrine Tumor 		11 0 1 9.1E-02 0 0
CUI: C0270458
Disease: Severe major depression with psychotic features
Severe major depression with psychotic features 		12 0 1 8.3E-02 0 0
CUI: C1820737
Disease: Temperature instability
Temperature instability 		12 0 1 8.3E-02 0 0
CUI: C1840333
Disease: Barakat syndrome
Barakat syndrome 		17 0 1 5.9E-02 0 0
CUI: C0809983
Disease: Schizophrenia and related disorders
Schizophrenia and related disorders 		20 0 1 5.0E-02 0 0
CUI: C0152115
Disease: Lingual-Facial-Buccal Dyskinesia
Lingual-Facial-Buccal Dyskinesia 		26 0 1 3.8E-02 0 0
CUI: C0231688
Disease: Gait, Shuffling
Gait, Shuffling 		28 0 1 3.6E-02 0 0
CUI: C0242423
Disease: Ramsay Hunt Paralysis Syndrome
Ramsay Hunt Paralysis Syndrome 		28 0 1 3.6E-02 0 0
CUI: C0752097
Disease: Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Juvenile Parkinson Disease 		28 0 1 3.6E-02 0 0
CUI: C0752101
Disease: Parkinsonism, Experimental
Parkinsonism, Experimental 		28 0 1 3.6E-02 0 0
CUI: C0752104
Disease: Familial Juvenile Parkinsonism
Familial Juvenile Parkinsonism 		28 0 1 3.6E-02 0 0
CUI: C1851920
Disease: Dopa-Responsive Dystonia
Dopa-Responsive Dystonia 		28 0 1 3.6E-02 0 0
CUI: C0038450
Disease: Stridor
Stridor 		31 0 1 3.2E-02 0 0
CUI: C0813217
Disease: Expressionless face
Expressionless face 		31 0 1 3.2E-02 0 0
CUI: C0752100
Disease: Autosomal Recessive Parkinsonism
Autosomal Recessive Parkinsonism 		33 0 1 3.0E-02 0 0
CUI: C0235032
Disease: Neurotoxicity Syndromes
Neurotoxicity Syndromes 		34 0 1 2.9E-02 0 0
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
Autosomal Dominant Parkinsonism 		34 0 1 2.9E-02 0 0