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: C0750992
Disease: Catatonia, Malignant
Catatonia, Malignant 		5 0 3 0.25 0 0
CUI: C4317093
Disease: Reduced factor XI activity
Reduced factor XI activity 		7 0 3 0.21 0 0
CUI: C4317295
Disease: Congenital disorder of glycosylation type 1s
Congenital disorder of glycosylation type 1s 		19 0 5 0.21 0 0
CUI: C0268225
Disease: Aspartylglucosaminuria
Aspartylglucosaminuria 		9 0 3 0.19 0 0
CUI: C0027612
Disease: Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital, Hereditary, and Neonatal Diseases and Abnormalities 		12 0 3 0.16 0 0
CUI: C1865145
Disease: Congenital disorder of glycosylation type 1B
Congenital disorder of glycosylation type 1B 		5 0 2 0.15 0 0
CUI: C0920372
Disease: Carcinogenesis, Radiation
Carcinogenesis, Radiation 		13 0 3 0.15 0 0
CUI: C1862839
Disease: Anterior segment mesenchymal dysgenesis
Anterior segment mesenchymal dysgenesis 		13 0 3 0.15 0 0
CUI: C1263988
Disease: Hemolytic disorder
Hemolytic disorder 		15 0 3 0.14 0 0
CUI: C0014761
Disease: Erythroblastosis, Fetal
Erythroblastosis, Fetal 		16 0 3 0.13 0 0
CUI: C1837899
Disease: Type I transferrin isoform profile
Type I transferrin isoform profile 		16 0 3 0.13 0 0
CUI: C4551511
Disease: X-linked sideroblastic anemia
X-linked sideroblastic anemia 		16 0 3 0.13 0 0
CUI: C0234935
Disease: Acute urticaria
Acute urticaria 		17 0 3 0.12 0 0
CUI: C0454595
Disease: Motor speech disorder
Motor speech disorder 		8 0 2 0.12 0 0
CUI: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency 		27 0 4 0.12 0 0
CUI: C4317224
Disease: Congenital disorder of glycosylation type 1q
Congenital disorder of glycosylation type 1q 		9 0 2 0.12 0 0
CUI: C0025237
Disease: Melnick-Needles Syndrome
Melnick-Needles Syndrome 		23 0 3 1.0E-01 0 0
CUI: C0268278
Disease: Infantile GM 2 gangliosidosis
Infantile GM 2 gangliosidosis 		1 0 1 1.0E-01 0 0
CUI: C0342844
Disease: Disorder of glycoprotein metabolism
Disorder of glycoprotein metabolism 		1 0 1 1.0E-01 0 0
CUI: C1291610
Disease: Deficiency of mannose-6-phosphate isomerase
Deficiency of mannose-6-phosphate isomerase 		1 0 1 1.0E-01 0 0
CUI: C1704380
Disease: Distal Renal Tubular Acidosis
Distal Renal Tubular Acidosis 		23 0 3 1.0E-01 0 0
CUI: C1833699
Disease: Osteopoikilosis, Isolated
Osteopoikilosis, Isolated 		1 0 1 1.0E-01 0 0
CUI: C2930923
Disease: N-Acetylneuraminic acid storage disease
N-Acetylneuraminic acid storage disease 		1 0 1 1.0E-01 0 0
CUI: C2930997
Disease: Congenital disorder of glycosylation type 1C
Congenital disorder of glycosylation type 1C 		1 0 1 1.0E-01 0 0
CUI: C2931505
Disease: Mixed sclerosing bone dystrophy
Mixed sclerosing bone dystrophy 		1 0 1 1.0E-01 0 0