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 0.20 0 0
CUI: C0027341
Disease: Nail-Patella Syndrome
Nail-Patella Syndrome 		1 0 1 0.20 0 0
CUI: C0158489
Disease: Acquired clubfoot
Acquired clubfoot 		1 0 1 0.20 0 0
CUI: C0206064
Disease: Microvascular Angina
Microvascular Angina 		1 0 1 0.20 0 0
CUI: C0403548
Disease: Salcedo syndrome
Salcedo syndrome 		1 0 1 0.20 0 0
CUI: C0431886
Disease: Thumb in palm deformity
Thumb in palm deformity 		1 0 1 0.20 0 0
CUI: C0524948
Disease: Maxillofacial Abnormalities
Maxillofacial Abnormalities 		1 0 1 0.20 0 0
CUI: C0685786
Disease: Cleft mandible
Cleft mandible 		1 0 1 0.20 0 0
CUI: C0852077
Disease: Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders, Inherited 		1 0 1 0.20 0 0
CUI: C1148477
Disease: Deafness, Sudden
Deafness, Sudden 		1 0 1 0.20 0 0
CUI: C1849348
Disease: Richieri Costa Pereira syndrome
Richieri Costa Pereira syndrome 		1 0 1 0.20 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 0.20 0 0
CUI: C1856059
Disease: Mthfr Deficiency, Thermolabile Type
Mthfr Deficiency, Thermolabile Type 		1 0 1 0.20 0 0
CUI: C1856061
Disease: Methylenetetrahydrofolate reductase deficiency
Methylenetetrahydrofolate reductase deficiency 		1 0 1 0.20 0 0
CUI: C1861316
Disease: Radially deviated wrists
Radially deviated wrists 		1 0 1 0.20 0 0
CUI: C4017062
Disease: HOMOCYSTINURIA DUE TO MTHFR DEFICIENCY
HOMOCYSTINURIA DUE TO MTHFR DEFICIENCY 		1 0 1 0.20 0 0
CUI: C4303787
Disease: Ehlers-Danlos syndrome musculocontractural type
Ehlers-Danlos syndrome musculocontractural type 		1 0 1 0.20 0 0
CUI: C0031900
Disease: Pierre Robin Syndrome
Pierre Robin Syndrome 		2 0 1 0.17 0 0
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
Sinus Thrombosis, Intracranial 		2 0 1 0.17 0 0
CUI: C0040156
Disease: Thyrotoxicosis
Thyrotoxicosis 		2 0 1 0.17 0 0
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
Cervical Intraepithelial Neoplasia 		2 0 1 0.17 0 0
CUI: C0751500
Disease: Petrous Sinus Thrombophlebitis
Petrous Sinus Thrombophlebitis 		2 0 1 0.17 0 0
CUI: C0751501
Disease: Intracranial Sinus Thrombophlebitis
Intracranial Sinus Thrombophlebitis 		2 0 1 0.17 0 0
CUI: C0751502
Disease: Petrous Sinus Thrombosis
Petrous Sinus Thrombosis 		2 0 1 0.17 0 0
CUI: C1851100
Disease: LAURIN-SANDROW SYNDROME
LAURIN-SANDROW SYNDROME 		2 0 1 0.17 0 0