Source: CURATED ×
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: C0025312
Disease: Meningomyelocele
Meningomyelocele 		4 4 4 1.00 1 0.25
CUI: C0751316
Disease: Acquired Meningomyelocele
Acquired Meningomyelocele 		4 0 4 1.00 0 0
CUI: C0041408
Disease: Turner Syndrome
Turner Syndrome 		5 0 2 0.29 0 0
CUI: C0242526
Disease: Gonadal Dysgenesis, 45,X
Gonadal Dysgenesis, 45,X 		5 0 2 0.29 0 0
CUI: C1527168
Disease: Bonnevie-Ullrich Syndrome
Bonnevie-Ullrich Syndrome 		5 0 2 0.29 0 0
CUI: C0002390
Disease: Extrinsic allergic alveolitis
Extrinsic allergic alveolitis 		1 0 1 0.25 0 0
CUI: C0003493
Disease: Aortic Diseases
Aortic Diseases 		6 0 2 0.25 0 0
CUI: C0004045
Disease: Asphyxia Neonatorum
Asphyxia Neonatorum 		6 0 2 0.25 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden 		1 0 1 0.25 0 0
CUI: C0014866
Disease: Esophageal Stenosis
Esophageal Stenosis 		1 0 1 0.25 0 0
CUI: C0034535
Disease: Radiation Syndrome
Radiation Syndrome 		1 0 1 0.25 0 0
CUI: C0206064
Disease: Microvascular Angina
Microvascular Angina 		1 0 1 0.25 0 0
CUI: C0238461
Disease: Anaplastic thyroid carcinoma
Anaplastic thyroid carcinoma 		1 0 1 0.25 0 0
CUI: C0242992
Disease: Multiple Chemical Sensitivity
Multiple Chemical Sensitivity 		1 0 1 0.25 0 0
CUI: C0524948
Disease: Maxillofacial Abnormalities
Maxillofacial Abnormalities 		1 0 1 0.25 0 0
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		1 0 1 0.25 0 0
CUI: C1148477
Disease: Deafness, Sudden
Deafness, Sudden 		1 0 1 0.25 0 0
CUI: C1510432
Disease: Radiation Sickness
Radiation Sickness 		1 0 1 0.25 0 0
CUI: C1856058
Disease: HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY
HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY 		1 0 1 0.25 0 0
CUI: C1856059
Disease: Mthfr Deficiency, Thermolabile Type
Mthfr Deficiency, Thermolabile Type 		1 0 1 0.25 0 0
CUI: C1856061
Disease: Methylenetetrahydrofolate reductase deficiency
Methylenetetrahydrofolate reductase deficiency 		1 0 1 0.25 0 0
CUI: C2675128
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 (finding) 		1 0 1 0.25 0 0
CUI: C4017062
Disease: HOMOCYSTINURIA DUE TO MTHFR DEFICIENCY
HOMOCYSTINURIA DUE TO MTHFR DEFICIENCY 		1 0 1 0.25 0 0
CUI: C4551650
Disease: Esophageal Stricture
Esophageal Stricture 		1 0 1 0.25 0 0
CUI: C0018200
Disease: Granuloma, Respiratory Tract
Granuloma, Respiratory Tract 		2 0 1 0.20 0 0