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: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden 		1 0 1 0.50 0 0
CUI: C0206064
Disease: Microvascular Angina
Microvascular Angina 		1 0 1 0.50 0 0
CUI: C0524948
Disease: Maxillofacial Abnormalities
Maxillofacial Abnormalities 		1 0 1 0.50 0 0
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		1 0 1 0.50 0 0
CUI: C1148477
Disease: Deafness, Sudden
Deafness, Sudden 		1 0 1 0.50 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 0.50 0 0
CUI: C1856059
Disease: Mthfr Deficiency, Thermolabile Type
Mthfr Deficiency, Thermolabile Type 		1 0 1 0.50 0 0
CUI: C1856061
Disease: Methylenetetrahydrofolate reductase deficiency
Methylenetetrahydrofolate reductase deficiency 		1 0 1 0.50 0 0
CUI: C4017062
Disease: HOMOCYSTINURIA DUE TO MTHFR DEFICIENCY
HOMOCYSTINURIA DUE TO MTHFR DEFICIENCY 		1 0 1 0.50 0 0
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
Sinus Thrombosis, Intracranial 		2 0 1 0.33 0 0
CUI: C0040156
Disease: Thyrotoxicosis
Thyrotoxicosis 		2 0 1 0.33 0 0
CUI: C0751500
Disease: Petrous Sinus Thrombophlebitis
Petrous Sinus Thrombophlebitis 		2 0 1 0.33 0 0
CUI: C0751501
Disease: Intracranial Sinus Thrombophlebitis
Intracranial Sinus Thrombophlebitis 		2 0 1 0.33 0 0
CUI: C0751502
Disease: Petrous Sinus Thrombosis
Petrous Sinus Thrombosis 		2 0 1 0.33 0 0
CUI: C0851140
Disease: Carcinoma in situ of uterine cervix
Carcinoma in situ of uterine cervix 		6 0 2 0.33 0 0
CUI: C0037928
Disease: Spinal Cord Diseases
Spinal Cord Diseases 		3 0 1 0.25 0 0
CUI: C0162429
Disease: Malnutrition
Malnutrition 		3 0 1 0.25 0 0
CUI: C0002902
Disease: Anencephaly
Anencephaly 		4 0 1 0.20 0 0
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele 		4 0 1 0.20 0 0
CUI: C0086664
Disease: Myelocele
Myelocele 		4 0 1 0.20 0 0
CUI: C0751316
Disease: Acquired Meningomyelocele
Acquired Meningomyelocele 		4 0 1 0.20 0 0
CUI: C1866558
Disease: Neural tube defect, folate-sensitive
Neural tube defect, folate-sensitive 		4 0 1 0.20 0 0
CUI: C3160733
Disease: THROMBOPHILIA DUE TO THROMBIN DEFECT
THROMBOPHILIA DUE TO THROMBIN DEFECT 		4 0 1 0.20 0 0
CUI: C0001723
Disease: Affective Disorders, Psychotic
Affective Disorders, Psychotic 		5 0 1 0.17 0 0
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		5 0 1 0.17 0 0