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: C0432273
Disease: Worth disease
Worth disease
1 0 1 1.00 0 0
Metacarpal diaphyseal endosteal sclerosis
1 0 1 1.00 0 0
Metatarsal diaphyseal endosteal sclerosis
1 0 1 1.00 0 0
CUI: C1842154
Disease: Sclerotic vertebral body
Sclerotic vertebral body
1 0 1 1.00 0 0
CUI: C1843323
Disease: Van Buchem disease type 2
Van Buchem disease type 2
1 0 1 1.00 0 0
CUI: C1843330
Disease: OSTEOPETROSIS, AUTOSOMAL DOMINANT 1
OSTEOPETROSIS, AUTOSOMAL DOMINANT 1
1 0 1 1.00 0 0
BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 1
1 2 1 1.00 1 0.33
EXUDATIVE VITREORETINOPATHY 4 (disorder)
1 0 1 1.00 0 0
CUI: C3554669
Disease: Clavicular sclerosis
Clavicular sclerosis
1 0 1 1.00 0 0
EXUDATIVE VITREORETINOPATHY 4, AUTOSOMAL DOMINANT
1 0 1 1.00 0 0
EXUDATIVE VITREORETINOPATHY 4, AUTOSOMAL RECESSIVE
1 0 1 1.00 0 0
EXUDATIVE VITREORETINOPATHY 4, DIGENIC
1 0 1 1.00 0 0
Abnormality of the femoral neck or head region
1 0 1 1.00 0 0
Visual acuity light perception with projection
1 0 1 1.00 0 0
POLYCYSTIC LIVER DISEASE 4 WITH OR WITHOUT KIDNEY CYSTS
1 0 1 1.00 0 0
POLYCYSTIC LIVER DISEASE 4 WITH KIDNEY CYSTS
1 0 1 1.00 0 0
CUI: C0266981
Disease: Torus palatinus
Torus palatinus
2 0 1 0.50 0 0
CUI: C0271004
Disease: Absent anterior chamber of eye
Absent anterior chamber of eye
2 0 1 0.50 0 0
CUI: C1851406
Disease: Peripheral retinal avascularization
Peripheral retinal avascularization
2 0 1 0.50 0 0
CUI: C3824901
Disease: Osteoporosis in children
Osteoporosis in children
2 0 1 0.50 0 0
CUI: C0342885
Disease: Secondary hypercholesterolemia
Secondary hypercholesterolemia
3 0 1 0.33 0 0
CUI: C0344550
Disease: Congenital retinal fold
Congenital retinal fold
3 0 1 0.33 0 0
CUI: C0004608
Disease: Retinopathy background
Retinopathy background
4 0 1 0.25 0 0
CUI: C0154828
Disease: Traction detachment of retina
Traction detachment of retina
4 0 1 0.25 0 0
CUI: C4329692
Disease: Craniotubular Hyperostosis
Craniotubular Hyperostosis
4 0 1 0.25 0 0