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: C0221727
Disease: Pain in esophagus (finding)
Pain in esophagus (finding) 		1 0 1 7.7E-02 0 0
CUI: C0455938
Disease: Large adenoids
Large adenoids 		1 0 1 7.7E-02 0 0
CUI: C1332865
Disease: Cavernous Sinus Meningioma
Cavernous Sinus Meningioma 		1 0 1 7.7E-02 0 0
CUI: C1850309
Disease: Mildly elevated creatine phosphokinase
Mildly elevated creatine phosphokinase 		1 0 1 7.7E-02 0 0
CUI: C3267131
Disease: Psychogenic movement disorder
Psychogenic movement disorder 		1 0 1 7.7E-02 0 0
CUI: C3710741
Disease: Torticollis, familial
Torticollis, familial 		1 0 1 7.7E-02 0 0
CUI: C4016920
Disease: DYSTONIA 1, TORSION, LATE-ONSET
DYSTONIA 1, TORSION, LATE-ONSET 		1 0 1 7.7E-02 0 0
CUI: C4255079
Disease: Familial Hyperekplexia
Familial Hyperekplexia 		1 0 1 7.7E-02 0 0
CUI: C4280687
Disease: Upper limb muscle hypertrophy
Upper limb muscle hypertrophy 		1 0 1 7.7E-02 0 0
CUI: C4310633
Disease: DYSTONIA 28, CHILDHOOD-ONSET
DYSTONIA 28, CHILDHOOD-ONSET 		1 0 1 7.7E-02 0 0
CUI: C4310634
Disease: DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES
DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES 		1 6 1 7.7E-02 6 0.75
CUI: C4748786
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17 		1 0 1 7.7E-02 0 0
CUI: C0025183
Disease: Meige Syndrome
Meige Syndrome 		2 0 2 0.15 0 0
CUI: C0347071
Disease: Malignant neoplasm of other and unspecified sites
Malignant neoplasm of other and unspecified sites 		2 0 1 7.1E-02 0 0
CUI: C0393604
Disease: Isolated blepharospasm
Isolated blepharospasm 		2 0 1 7.1E-02 0 0
CUI: C0748605
Disease: nocturnal seizures
nocturnal seizures 		2 0 1 7.1E-02 0 0
CUI: C0750968
Disease: Central Nervous System Metabolic Disorders
Central Nervous System Metabolic Disorders 		2 0 1 7.1E-02 0 0
CUI: C0751743
Disease: Metabolic Disorder, Central Nervous System, Acquired
Metabolic Disorder, Central Nervous System, Acquired 		2 0 1 7.1E-02 0 0
CUI: C0751744
Disease: Brain Diseases, Metabolic, Acquired
Brain Diseases, Metabolic, Acquired 		2 0 1 7.1E-02 0 0
CUI: C1135773
Disease: Acquired Metabolic Diseases, Nervous System
Acquired Metabolic Diseases, Nervous System 		2 0 1 7.1E-02 0 0
CUI: C1835798
Disease: Anoperineal fistula
Anoperineal fistula 		2 0 1 7.1E-02 0 0
CUI: C1860216
Disease: Progressive choreoathetosis
Progressive choreoathetosis 		2 0 1 7.1E-02 0 0
CUI: C1861239
Disease: Plantar flexion contractures
Plantar flexion contractures 		2 0 1 7.1E-02 0 0
CUI: C1868705
Disease: Shone complex
Shone complex 		2 0 1 7.1E-02 0 0
CUI: C1969807
Disease: Dystonia, Focal, Task-Specific
Dystonia, Focal, Task-Specific 		2 0 1 7.1E-02 0 0