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: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 8.3E-02
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse 		0 1 0 0 1 9.1E-02
CUI: C2242712
Disease: Hyper LDL cholesterolaemia
Hyper LDL cholesterolaemia 		0 19 0 0 1 3.4E-02
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 9.1E-02
CUI: C1837142
Disease: Poor suck
Poor suck 		103 0 1 1.3E-03 0 0
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		87 0 1 1.4E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 1.4E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.4E-03 0 0
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		80 0 1 1.4E-03 0 0
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		75 0 1 1.4E-03 0 0
CUI: C3554617
Disease: Adducted thumb
Adducted thumb 		74 0 1 1.4E-03 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact 		73 0 1 1.4E-03 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 1 1.4E-03 0 0
CUI: C0741916
Disease: Cardiac defects
Cardiac defects 		62 0 1 1.4E-03 0 0
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL 		61 0 1 1.4E-03 0 0
CUI: C0277959
Disease: Coarse hair
Coarse hair 		60 0 1 1.4E-03 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function 		59 0 1 1.4E-03 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 1.4E-03 0 0
CUI: C0751882
Disease: Myasthenic Syndromes, Congenital
Myasthenic Syndromes, Congenital 		57 0 1 1.4E-03 0 0
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 0 1 1.4E-03 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		55 0 1 1.4E-03 0 0
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		55 0 1 1.4E-03 0 0
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem 		55 0 1 1.4E-03 0 0
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		55 0 1 1.4E-03 0 0
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		54 0 1 1.4E-03 0 0