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 5.6E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.0E-01
CUI: C0036904
Disease: Sexual desire disorder
Sexual desire disorder 		0 1 0 0 1 1.0E-01
CUI: C0206042
Disease: Fatal Familial Insomnia
Fatal Familial Insomnia 		0 16 0 0 1 4.0E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 1 7.1E-02
CUI: C1405458
Disease: Language Problems
Language Problems 		0 2 0 0 1 9.1E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		0 9 0 0 1 5.6E-02
CUI: C1864112
Disease: HUNTINGTON DISEASE-LIKE 1
HUNTINGTON DISEASE-LIKE 1 		0 4 0 0 1 7.7E-02
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0 3 0 0 1 8.3E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.0E-01
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.0E-01
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 9.1E-02
CUI: C4275003
Disease: Familial Creutzfeldt-Jakob
Familial Creutzfeldt-Jakob 		0 1 0 0 1 1.0E-01
CUI: C4551693
Disease: Wolfram Syndrome 1
Wolfram Syndrome 1 		0 36 0 0 1 2.2E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 8.3E-02
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		291 0 1 2.2E-03 0 0
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		223 0 1 2.6E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 2.7E-03 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		186 0 1 2.9E-03 0 0
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE 		175 0 1 3.0E-03 0 0
CUI: C3714745
Disease: Malabsorption
Malabsorption 		175 0 1 3.0E-03 0 0
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers 		171 0 1 3.0E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 3.0E-03 0 0
CUI: C0162298
Disease: Joint stiffness
Joint stiffness 		163 0 1 3.1E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 3.1E-03 0 0