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: C0543515
Disease: Sucrase deficiency
Sucrase deficiency 		1 0 1 0.50 0 0
CUI: C0699848
Disease: Disaccharidase deficiency
Disaccharidase deficiency 		1 0 1 0.50 0 0
CUI: C3665817
Disease: Hypocarnitinaemia
Hypocarnitinaemia 		1 0 1 0.50 0 0
CUI: C0555970
Disease: Nasal infection
Nasal infection 		2 0 1 0.33 0 0
CUI: C0545044
Disease: Acrokeratoelastoidosis of Costa
Acrokeratoelastoidosis of Costa 		3 0 1 0.25 0 0
CUI: C0149821
Disease: ACUTE ALCOHOL WITHDRAWAL
ACUTE ALCOHOL WITHDRAWAL 		4 0 1 0.20 0 0
CUI: C0259817
Disease: Xerosis
Xerosis 		4 0 1 0.20 0 0
CUI: C0546343
Disease: Mucosal erosion
Mucosal erosion 		4 0 1 0.20 0 0
CUI: C0751173
Disease: Glycogen Storage Disease Type II, Infantile
Glycogen Storage Disease Type II, Infantile 		4 0 1 0.20 0 0
CUI: C0795824
Disease: Chromosome 8, monosomy 8p
Chromosome 8, monosomy 8p 		4 0 1 0.20 0 0
CUI: C0264492
Disease: Chronic respiratory failure
Chronic respiratory failure 		5 0 1 0.17 0 0
CUI: C0264652
Disease: Hypertensive heart failure
Hypertensive heart failure 		5 0 1 0.17 0 0
CUI: C2673697
Disease: Dystonia with Cerebellar Atrophy
Dystonia with Cerebellar Atrophy 		5 0 1 0.17 0 0
CUI: C1521897
Disease: Mature T ALL
Mature T ALL 		6 0 1 0.14 0 0
CUI: C3888924
Disease: Glycogen storage disease due to acid maltase deficiency, infantile onset
Glycogen storage disease due to acid maltase deficiency, infantile onset 		7 0 1 0.12 0 0
CUI: C0342753
Disease: Glycogen storage disease due to acid maltase deficiency, late-onset
Glycogen storage disease due to acid maltase deficiency, late-onset 		8 0 1 0.11 0 0
CUI: C0030491
Disease: Parapsoriasis
Parapsoriasis 		10 0 1 9.1E-02 0 0
CUI: C0038187
Disease: Starvation
Starvation 		10 0 1 9.1E-02 0 0
CUI: C0852262
Disease: Placental abnormalities (excl neoplasms)
Placental abnormalities (excl neoplasms) 		12 0 1 7.7E-02 0 0
CUI: C1960458
Disease: Differentiation syndrome due to and following chemotherapy co-occurrent with acute promyelocytic leukemia
Differentiation syndrome due to and following chemotherapy co-occurrent with acute promyelocytic leukemia 		12 0 1 7.7E-02 0 0
CUI: C0795878
Disease: Monosomy 22
Monosomy 22 		14 0 1 6.7E-02 0 0
CUI: C4288892
Disease: Infant Acute Undifferentiated Leukemia
Infant Acute Undifferentiated Leukemia 		14 0 1 6.7E-02 0 0
CUI: C1838625
Disease: Warburg Sjo Fledelius syndrome
Warburg Sjo Fledelius syndrome 		16 0 1 5.9E-02 0 0
CUI: C2675519
Disease: Hypoadiponectinemia
Hypoadiponectinemia 		16 0 1 5.9E-02 0 0
CUI: C0302362
Disease: Brucella melitensis infection
Brucella melitensis infection 		17 0 1 5.6E-02 0 0