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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 5.0E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 8.3E-02
CUI: C0036904
Disease: Sexual desire disorder
Sexual desire disorder 		0 1 0 0 1 8.3E-02
CUI: C0206042
Disease: Fatal Familial Insomnia
Fatal Familial Insomnia 		0 16 0 0 1 3.7E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 1 6.2E-02
CUI: C1405458
Disease: Language Problems
Language Problems 		0 2 0 0 1 7.7E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		0 9 0 0 1 5.0E-02
CUI: C1864112
Disease: HUNTINGTON DISEASE-LIKE 1
HUNTINGTON DISEASE-LIKE 1 		0 4 0 0 1 6.7E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0 3 0 0 1 7.1E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 8.3E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 8.3E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 7.7E-02
CUI: C4275003
Disease: Familial Creutzfeldt-Jakob
Familial Creutzfeldt-Jakob 		0 1 0 0 1 8.3E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 5.0E-02
CUI: C4694057
Disease: Taq1A POLYMORPHISM
Taq1A POLYMORPHISM 		0 14 0 0 2 8.3E-02
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		291 0 1 2.2E-03 0 0
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		272 0 1 2.3E-03 0 0
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		223 0 1 2.5E-03 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears 		223 0 1 2.5E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 2.6E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		208 0 1 2.6E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 0 1 2.8E-03 0 0
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear 		176 0 1 2.9E-03 0 0
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE 		175 0 1 2.9E-03 0 0
CUI: C3714745
Disease: Malabsorption
Malabsorption 		175 0 1 2.9E-03 0 0