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: C0010038
Disease: Corneal Opacity
Corneal Opacity 		3 0 1 6.2E-03 0 0
CUI: C0010043
Disease: Corneal Ulcer
Corneal Ulcer 		1 0 1 6.3E-03 0 0
CUI: C0010051
Disease: Coronary Aneurysm
Coronary Aneurysm 		1 0 1 6.3E-03 0 0
CUI: C0010276
Disease: Craniopharyngioma
Craniopharyngioma 		2 0 1 6.2E-03 0 0
CUI: C0010606
Disease: Adenoid Cystic Carcinoma
Adenoid Cystic Carcinoma 		11 0 1 5.9E-03 0 0
CUI: C0011053
Disease: Deafness
Deafness 		23 0 1 5.5E-03 0 0
CUI: C0011813
Disease: Dextrocardia
Dextrocardia 		6 0 1 6.1E-03 0 0
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		6 0 1 6.1E-03 0 0
CUI: C0011981
Disease: Diaphragmatic Eventration
Diaphragmatic Eventration 		6 0 1 6.1E-03 0 0
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle 		6 0 1 6.1E-03 0 0
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		6 0 1 6.1E-03 0 0
CUI: C0014170
Disease: Endometrial Neoplasms
Endometrial Neoplasms 		2 0 1 6.2E-03 0 0
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial 		8 0 2 1.2E-02 0 0
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease 		2 0 1 6.2E-03 0 0
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		22 0 4 2.2E-02 0 0
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple 		4 0 1 6.1E-03 0 0
CUI: C0018671
Disease: Head and Neck Neoplasms
Head and Neck Neoplasms 		4 0 1 6.1E-03 0 0
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects 		4 0 1 6.1E-03 0 0
CUI: C0018799
Disease: Heart Diseases
Heart Diseases 		1 0 1 6.3E-03 0 0
CUI: C0018808
Disease: Heart murmur
Heart murmur 		11 0 2 1.2E-02 0 0
CUI: C0018932
Disease: Hematochezia
Hematochezia 		2 0 1 6.2E-03 0 0
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal 		13 0 2 1.2E-02 0 0
CUI: C0019322
Disease: Umbilical hernia
Umbilical hernia 		17 0 1 5.7E-03 0 0
CUI: C0020072
Disease: Hereditary Sensory Autonomic Neuropathy, Type 2
Hereditary Sensory Autonomic Neuropathy, Type 2 		3 0 1 6.2E-03 0 0
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		25 0 2 1.1E-02 0 0