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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.6E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 2.6E-02
CUI: C3553462
Disease: INFLUENZA, SEVERE, SUSCEPTIBILITY TO
INFLUENZA, SEVERE, SUSCEPTIBILITY TO 		0 1 0 0 1 2.6E-02
CUI: C3665951
Disease: Influenza due to Influenza A virus subtype H7N9
Influenza due to Influenza A virus subtype H7N9 		0 3 0 0 1 2.4E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.6E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 2.4E-02
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 9.5E-04 0 0
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		62 0 1 9.6E-04 0 0
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		62 0 1 9.6E-04 0 0
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		50 0 1 9.7E-04 0 0
CUI: C1865037
Disease: Cone-shaped epiphysis
Cone-shaped epiphysis 		49 0 1 9.8E-04 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 9.8E-04 0 0
CUI: C0432333
Disease: Abnormal dermatoglyphic pattern
Abnormal dermatoglyphic pattern 		44 0 1 9.8E-04 0 0
CUI: C0685840
Disease: Congenital hypoplasia of ovary
Congenital hypoplasia of ovary 		44 0 1 9.8E-04 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance 		44 0 1 9.8E-04 0 0
CUI: C0266399
Disease: Infantile uterus
Infantile uterus 		43 0 1 9.8E-04 0 0
CUI: C4551906
Disease: Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		43 0 1 9.8E-04 0 0
CUI: C1839797
Disease: Deep philtrum
Deep philtrum 		42 0 1 9.8E-04 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 1 9.8E-04 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 1 9.8E-04 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 1 9.8E-04 0 0
CUI: C0432163
Disease: Defect of vertebral segmentation
Defect of vertebral segmentation 		40 0 1 9.8E-04 0 0
CUI: C0266174
Disease: Duodenal atresia
Duodenal atresia 		39 0 1 9.9E-04 0 0
CUI: C0524957
Disease: Corneal Topography
Corneal Topography 		39 0 1 9.9E-04 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly 		37 0 1 9.9E-04 0 0