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: C0241181
Disease: Fragile skin
Fragile skin 		3 5 2 0.22 1 8.3E-02
CUI: C0004045
Disease: Asphyxia Neonatorum
Asphyxia Neonatorum 		4 4 2 0.20 2 0.20
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		6 11 2 0.17 2 0.12
CUI: C0026266
Disease: Mitral Valve Insufficiency
Mitral Valve Insufficiency 		7 11 2 0.15 1 5.6E-02
CUI: C1837731
Disease: Overfolded helix
Overfolded helix 		7 7 2 0.15 2 0.15
CUI: C1858085
Disease: Malar flattening
Malar flattening 		7 12 2 0.15 2 0.11
CUI: C0004106
Disease: Astigmatism
Astigmatism 		15 14 3 0.15 2 1.0E-01
CUI: C0020490
Disease: Hyperopia
Hyperopia 		16 17 3 0.14 3 0.14
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		16 17 3 0.14 3 0.14
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		8 19 2 0.14 1 3.8E-02
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly 		9 24 2 0.13 2 6.7E-02
CUI: C0040433
Disease: Tooth Crowding
Tooth Crowding 		9 19 2 0.13 2 8.0E-02
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		9 11 2 0.13 2 0.12
CUI: C4072908
Disease: Induced vaginal delivery
Induced vaginal delivery 		9 10 2 0.13 2 0.12
CUI: C0003486
Disease: Aortic Aneurysm
Aortic Aneurysm 		1 0 1 0.12 0 0
CUI: C0012736
Disease: Dissecting aortic aneurysm
Dissecting aortic aneurysm 		1 0 1 0.12 0 0
CUI: C0016873
Disease: Fused Teeth
Fused Teeth 		1 1 1 0.12 1 0.12
CUI: C0020500
Disease: Hyperoxaluria
Hyperoxaluria 		1 1 1 0.12 1 0.12
CUI: C0154850
Disease: Cystoid macular retinal degeneration
Cystoid macular retinal degeneration 		1 1 1 0.12 1 0.12
CUI: C0238210
Disease: Malrotation of kidney
Malrotation of kidney 		1 1 1 0.12 1 0.12
CUI: C0239574
Disease: Low grade fever
Low grade fever 		1 1 1 0.12 1 0.12
CUI: C0240231
Disease: Fractures of the long bones
Fractures of the long bones 		1 1 1 0.12 1 0.12
CUI: C0241165
Disease: Thick skin
Thick skin 		1 0 1 0.12 0 0
CUI: C0265287
Disease: Acromicric Dysplasia
Acromicric Dysplasia 		1 0 1 0.12 0 0
CUI: C0265290
Disease: Metaphyseal chondrodysplasia
Metaphyseal chondrodysplasia 		1 0 1 0.12 0 0