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: C0037277
Disease: Skin Diseases, Genetic
Skin Diseases, Genetic 		57 0 1 2.5E-03 0 0
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		57 0 1 2.5E-03 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 2.5E-03 0 0
CUI: C0751882
Disease: Myasthenic Syndromes, Congenital
Myasthenic Syndromes, Congenital 		57 0 1 2.5E-03 0 0
CUI: C1302790
Disease: Congenital malformation syndrome
Congenital malformation syndrome 		57 0 1 2.5E-03 0 0
CUI: C1858036
Disease: Periorbital fullness
Periorbital fullness 		57 0 1 2.5E-03 0 0
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		55 0 1 2.5E-03 0 0
CUI: C1389016
Disease: ATRIOVENTRICULAR CANAL DEFECT
ATRIOVENTRICULAR CANAL DEFECT 		55 0 1 2.5E-03 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign 		54 0 1 2.5E-03 0 0
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		54 0 1 2.5E-03 0 0
CUI: C0268287
Disease: Deficiency of steroid 21-monooxygenase
Deficiency of steroid 21-monooxygenase 		54 0 1 2.5E-03 0 0
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		54 0 1 2.5E-03 0 0
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		54 0 1 2.5E-03 0 0
CUI: C0017979
Disease: Glycosuria
Glycosuria 		53 0 1 2.5E-03 0 0
CUI: C0271979
Disease: Thalassemia Intermedia
Thalassemia Intermedia 		53 0 1 2.5E-03 0 0
CUI: C0337443
Disease: Sodium measurement
Sodium measurement 		53 0 1 2.5E-03 0 0
CUI: C0406208
Disease: Suntan
Suntan 		53 0 1 2.5E-03 0 0
CUI: C1839546
Disease: Microretrognathia
Microretrognathia 		53 0 1 2.5E-03 0 0
CUI: C0001126
Disease: Renal tubular acidosis
Renal tubular acidosis 		52 0 1 2.5E-03 0 0
CUI: C0730292
Disease: Macular dystrophy
Macular dystrophy 		52 0 1 2.5E-03 0 0
CUI: C4024748
Disease: Aplasia/Hypoplasia of the iris
Aplasia/Hypoplasia of the iris 		52 0 1 2.5E-03 0 0
CUI: C0013592
Disease: Ectropion
Ectropion 		50 0 1 2.5E-03 0 0
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		50 0 1 2.5E-03 0 0
CUI: C0238395
Disease: Male Pseudohermaphroditism
Male Pseudohermaphroditism 		50 0 1 2.5E-03 0 0
CUI: C1860614
Disease: ULNAR HYPOPLASIA
ULNAR HYPOPLASIA 		50 0 1 2.5E-03 0 0