Source: ALL
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: C0231554
Disease: Osteoid formation disorder
Osteoid formation disorder 		1 0 1 0.33 0 0
CUI: C1290783
Disease: Peripheral ossifying fibroma
Peripheral ossifying fibroma 		1 0 1 0.33 0 0
CUI: C1859709
Disease: Kuskokwim disease
Kuskokwim disease 		1 0 1 0.33 0 0
CUI: C3151218
Disease: OSTEOGENESIS IMPERFECTA, TYPE XI
OSTEOGENESIS IMPERFECTA, TYPE XI 		1 3 1 0.33 1 0.14
CUI: C3553887
Disease: OSTEOGENESIS IMPERFECTA, TYPE XIII
OSTEOGENESIS IMPERFECTA, TYPE XIII 		1 0 1 0.33 0 0
CUI: C3839326
Disease: Kuskokwim syndrome
Kuskokwim syndrome 		1 0 1 0.33 0 0
CUI: C1836602
Disease: Bruck syndrome 2
Bruck syndrome 2 		2 0 1 0.25 0 0
CUI: C1850168
Disease: Bruck syndrome 1
Bruck syndrome 1 		2 8 1 0.25 2 0.18
CUI: C0031382
Disease: PHENCYCLIDINE/ARYLCYCLOHEXYLAMINE ABUSE
PHENCYCLIDINE/ARYLCYCLOHEXYLAMINE ABUSE 		3 0 1 0.20 0 0
CUI: C0268363
Disease: Osteogenesis imperfecta type IV (disorder)
Osteogenesis imperfecta type IV (disorder) 		12 0 2 0.15 0 0
CUI: C0432253
Disease: Bruck syndrome
Bruck syndrome 		6 0 1 0.12 0 0
CUI: C3888924
Disease: Glycogen storage disease due to acid maltase deficiency, infantile onset
Glycogen storage disease due to acid maltase deficiency, infantile onset 		7 0 1 0.11 0 0
CUI: C0268362
Disease: Osteogenesis imperfecta type III (disorder)
Osteogenesis imperfecta type III (disorder) 		18 0 2 0.11 0 0
CUI: C1695776
Disease: Vertebral wedging
Vertebral wedging 		8 0 1 1.0E-01 0 0
CUI: C1857484
Disease: Brachyturricephaly
Brachyturricephaly 		9 0 1 9.1E-02 0 0
CUI: C0409495
Disease: Protrusio acetabuli
Protrusio acetabuli 		10 0 1 8.3E-02 0 0
CUI: C4551680
Disease: Generalized osteoporosis
Generalized osteoporosis 		13 0 1 6.7E-02 0 0
CUI: C1842138
Disease: Progressive hearing impairment
Progressive hearing impairment 		14 0 1 6.2E-02 0 0
CUI: C0079294
Disease: Epidermolysis Bullosa Dystrophica
Epidermolysis Bullosa Dystrophica 		15 0 1 5.9E-02 0 0
CUI: C0011436
Disease: Dentinogenesis Imperfecta
Dentinogenesis Imperfecta 		35 0 2 5.6E-02 0 0
CUI: C0023003
Disease: Langer-Giedion Syndrome
Langer-Giedion Syndrome 		16 0 1 5.6E-02 0 0
CUI: C1856087
Disease: Biconcave vertebral bodies
Biconcave vertebral bodies 		16 0 1 5.6E-02 0 0
CUI: C0851886
Disease: Pneumocystis Infections
Pneumocystis Infections 		18 0 1 5.0E-02 0 0
CUI: C0235889
Disease: Arthritis aggravated
Arthritis aggravated 		19 0 1 4.8E-02 0 0
CUI: C0473527
Disease: Hypoalphalipoproteinemias
Hypoalphalipoproteinemias 		20 0 1 4.5E-02 0 0