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: C0006325
Disease: Bruxism
Bruxism
0 9 0 0 1 5.6E-02
CUI: C0009398
Disease: Color vision defect
Color vision defect
0 4 0 0 2 0.17
CUI: C0020875
Disease: Ileal Diseases
Ileal Diseases
0 7 0 0 1 6.2E-02
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy
0 15 0 0 1 4.2E-02
CUI: C0221163
Disease: Motor Disorders
Motor Disorders
0 2 0 0 1 9.1E-02
CUI: C0234253
Disease: Rest pain
Rest pain
0 1 0 0 1 1.0E-01
CUI: C0392156
Disease: Akathisia
Akathisia
0 12 0 0 1 4.8E-02
CUI: C0745031
Disease: homicidal
homicidal
0 2 0 0 1 9.1E-02
CUI: C1282916
Disease: Secondary Raynaud's phenomenon
Secondary Raynaud's phenomenon
0 1 0 0 1 1.0E-01
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse
0 1 0 0 1 1.0E-01
Frequent episodic tension-type headache
0 1 0 0 1 1.0E-01
Large-artery atherosclerosis (embolus/thrombosis)
0 35 0 0 1 2.3E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
656 0 1 1.5E-03 0 0
CUI: C0037274
Disease: Dermatologic disorders
Dermatologic disorders
617 0 1 1.6E-03 0 0
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
610 0 1 1.6E-03 0 0
Red cell distribution width determination
593 0 1 1.6E-03 0 0
RDW - Red blood cell distribution width result
593 0 1 1.6E-03 0 0
Delayed speech and language development
560 0 1 1.7E-03 0 0
Congenital contractural arachnodactyly
559 0 1 1.7E-03 0 0
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
539 0 1 1.8E-03 0 0
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
Gastrointestinal Stromal Tumors
538 0 1 1.8E-03 0 0
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate
497 0 1 1.9E-03 0 0
CUI: C0002170
Disease: Alopecia
Alopecia
491 0 1 1.9E-03 0 0
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
6385 0 13 2.0E-03 0 0
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
955 0 2 2.0E-03 0 0