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: C0029928
Disease: Ovarian Diseases
Ovarian Diseases 		0 5 0 0 1 7.5E-04
CUI: C0265514
Disease: Dermatofibrosis lenticularis disseminata
Dermatofibrosis lenticularis disseminata 		0 3 0 0 1 7.6E-04
CUI: C0276340
Disease: Respiratory syncytial virus bronchiolitis
Respiratory syncytial virus bronchiolitis 		0 1 0 0 1 7.6E-04
CUI: C0947912
Disease: Myasthenias
Myasthenias 		0 3 0 0 1 7.6E-04
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 7.6E-04
CUI: C1840598
Disease: FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 2
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 2 		0 1 0 0 1 7.6E-04
CUI: C2825910
Disease: Stem Cell Factor Measurement
Stem Cell Factor Measurement 		0 8 0 0 1 7.5E-04
CUI: C3812686
Disease: Interleukin 1 Receptor Antagonist Measurement
Interleukin 1 Receptor Antagonist Measurement 		0 11 0 0 1 7.5E-04
CUI: C4285782
Disease: Kinesiophobia
Kinesiophobia 		0 1 0 0 1 7.6E-04
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal 		130 0 1 1.2E-03 0 0
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies 		121 0 1 1.2E-03 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities 		112 0 1 1.3E-03 0 0
CUI: C0282577
Disease: Congenital Disorders of Glycosylation
Congenital Disorders of Glycosylation 		102 0 1 1.3E-03 0 0
CUI: C0023015
Disease: Language Disorders
Language Disorders 		94 0 1 1.3E-03 0 0
CUI: C0041349
Disease: Nephritis, Tubulointerstitial
Nephritis, Tubulointerstitial 		92 0 1 1.3E-03 0 0
CUI: C3501843
Disease: Nonmedullary Thyroid Carcinoma
Nonmedullary Thyroid Carcinoma 		89 0 1 1.3E-03 0 0
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		87 0 1 1.3E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 1.3E-03 0 0
CUI: C0917713
Disease: Becker Muscular Dystrophy
Becker Muscular Dystrophy 		86 0 1 1.3E-03 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis 		85 0 1 1.3E-03 0 0
CUI: C0339525
Disease: Autosomal dominant retinitis pigmentosa
Autosomal dominant retinitis pigmentosa 		85 0 1 1.3E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.3E-03 0 0
CUI: C0085437
Disease: Meningitis, Bacterial
Meningitis, Bacterial 		81 0 1 1.3E-03 0 0
CUI: C0524662
Disease: Opiate Addiction
Opiate Addiction 		81 0 1 1.3E-03 0 0
CUI: C0040588
Disease: Tracheoesophageal Fistula
Tracheoesophageal Fistula 		80 0 1 1.3E-03 0 0