Source: CLINVAR ×
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: C0010606
Disease: Adenoid Cystic Carcinoma
Adenoid Cystic Carcinoma 		11 0 2 1.5E-02 0 0
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome 		9 0 1 7.4E-03 0 0
CUI: C0011053
Disease: Deafness
Deafness 		23 0 1 6.7E-03 0 0
CUI: C0011071
Disease: Sudden death
Sudden death 		4 0 2 1.5E-02 0 0
CUI: C0011175
Disease: Dehydration
Dehydration 		2 0 1 7.8E-03 0 0
CUI: C0011436
Disease: Dentinogenesis Imperfecta
Dentinogenesis Imperfecta 		2 0 1 7.8E-03 0 0
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		6 0 1 7.5E-03 0 0
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		6 0 1 7.5E-03 0 0
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		29 0 1 6.4E-03 0 0
CUI: C0011981
Disease: Diaphragmatic Eventration
Diaphragmatic Eventration 		6 0 1 7.5E-03 0 0
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle 		6 0 1 7.5E-03 0 0
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial 		8 0 4 3.0E-02 0 0
CUI: C0014805
Disease: Primary Erythermalgia
Primary Erythermalgia 		2 0 1 7.8E-03 0 0
CUI: C0014850
Disease: Esophageal Atresia
Esophageal Atresia 		2 0 1 7.8E-03 0 0
CUI: C0016506
Disease: Foot Deformities
Foot Deformities 		3 0 1 7.7E-03 0 0
CUI: C0017601
Disease: Glaucoma
Glaucoma 		6 0 1 7.5E-03 0 0
CUI: C0017639
Disease: Gliosis
Gliosis 		4 0 2 1.5E-02 0 0
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple 		4 0 1 7.6E-03 0 0
CUI: C0018621
Disease: Hay fever
Hay fever 		1 0 1 7.8E-03 0 0
CUI: C0018671
Disease: Head and Neck Neoplasms
Head and Neck Neoplasms 		4 0 1 7.6E-03 0 0
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		8 0 1 7.4E-03 0 0
CUI: C0018989
Disease: Hemiparesis
Hemiparesis 		4 0 1 7.6E-03 0 0
CUI: C0018991
Disease: Hemiplegia
Hemiplegia 		3 0 1 7.7E-03 0 0
CUI: C0020072
Disease: Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Autonomic Neuropathy, Type 2 		3 0 1 7.7E-03 0 0
CUI: C0020497
Disease: Cortical Congenital Hyperostosis
Cortical Congenital Hyperostosis 		2 0 1 7.8E-03 0 0