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 1.7E-03
CUI: C0033923
Disease: Psychomotor Performance
Psychomotor Performance 		0 1 0 0 1 1.7E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.7E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 1.7E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 1.7E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.7E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 1.7E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 1.7E-03
CUI: C1837217
Disease: Cleft lip, isolated
Cleft lip, isolated 		0 2 0 0 1 1.7E-03
CUI: C1852324
Disease: ALDOSTERONE TO RENIN RATIO, INCREASED
ALDOSTERONE TO RENIN RATIO, INCREASED 		0 1 0 0 1 1.7E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.7E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 1.7E-03
CUI: C4755308
Disease: Familial cervical artery dissection
Familial cervical artery dissection 		0 2 0 0 1 1.7E-03
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia 		100 0 1 9.6E-04 0 0
CUI: C1850456
Disease: Progressive microcephaly
Progressive microcephaly 		67 0 1 1.0E-03 0 0
CUI: C3501844
Disease: Familial Nonmedullary Thyroid Cancer
Familial Nonmedullary Thyroid Cancer 		66 0 1 1.0E-03 0 0
CUI: C0431659
Disease: Hypoplasia of scrotum
Hypoplasia of scrotum 		57 0 1 1.0E-03 0 0
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 0 1 1.0E-03 0 0
CUI: C0406208
Disease: Suntan
Suntan 		53 0 1 1.0E-03 0 0
CUI: C0575059
Disease: Spastic tetraparesis
Spastic tetraparesis 		50 0 1 1.0E-03 0 0
CUI: C0032987
Disease: Ectopic Pregnancy
Ectopic Pregnancy 		48 0 1 1.0E-03 0 0
CUI: C4024926
Disease: Focal T2 hyperintense basal ganglia lesion
Focal T2 hyperintense basal ganglia lesion 		46 0 1 1.0E-03 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 1.0E-03 0 0
CUI: C1866190
Disease: Atresia of the external auditory canal
Atresia of the external auditory canal 		44 0 1 1.0E-03 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central 		43 0 1 1.0E-03 0 0