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: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology 		70 0 1 1.5E-03 0 0
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		58 0 1 1.5E-03 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 1.5E-03 0 0
CUI: C0869220
Disease: Adverse effects, not elsewhere classified
Adverse effects, not elsewhere classified 		55 0 1 1.5E-03 0 0
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		54 0 1 1.5E-03 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign 		54 0 1 1.5E-03 0 0
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		53 0 1 1.5E-03 0 0
CUI: C0730292
Disease: Macular dystrophy
Macular dystrophy 		52 0 1 1.5E-03 0 0
CUI: C0240479
Disease: Neck muscle weakness
Neck muscle weakness 		49 0 1 1.5E-03 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 1.5E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 1 1.5E-03 0 0
CUI: C0423250
Disease: Corneal stromal opacities
Corneal stromal opacities 		46 0 1 1.5E-03 0 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe 		46 0 1 1.5E-03 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 1.5E-03 0 0
CUI: C4722328
Disease: Hereditary Prostate Carcinoma
Hereditary Prostate Carcinoma 		45 0 1 1.5E-03 0 0
CUI: C1866190
Disease: Atresia of the external auditory canal
Atresia of the external auditory canal 		44 0 1 1.5E-03 0 0
CUI: C2931038
Disease: Pancreatic carcinoma, familial
Pancreatic carcinoma, familial 		43 0 1 1.5E-03 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 1.5E-03 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 1 1.5E-03 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 1 1.5E-03 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 1 1.5E-03 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		40 0 1 1.5E-03 0 0
CUI: C1285654
Disease: Memory performance
Memory performance 		40 0 1 1.5E-03 0 0
CUI: C0020256
Disease: Congenital Hydrocephalus
Congenital Hydrocephalus 		39 0 1 1.5E-03 0 0
CUI: C0029489
Disease: Other alopecia
Other alopecia 		39 0 1 1.5E-03 0 0