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: C0023931
Disease: Lobstein Disease
Lobstein Disease
5 255 4 0.67 4 1.2E-02
Osteogenesis imperfecta type III (disorder)
11 65 5 0.45 6 4.0E-02
EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE
2 0 2 0.40 0 0
EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1
2 0 2 0.40 0 0
Osteogenesis imperfecta type IV (disorder)
10 59 4 0.36 4 2.8E-02
CUI: C0029434
Disease: Osteogenesis Imperfecta
Osteogenesis Imperfecta
13 52 4 0.29 2 1.4E-02
CUI: C0013720
Disease: Ehlers-Danlos Syndrome
Ehlers-Danlos Syndrome
5 0 2 0.25 0 0
CUI: C0020497
Disease: Cortical Congenital Hyperostosis
Cortical Congenital Hyperostosis
1 0 1 0.20 0 0
CUI: C0029118
Disease: Opportunistic Infections
Opportunistic Infections
1 0 1 0.20 0 0
OSTEOGENESIS IMPERFECTA, TYPE IX (disorder)
1 0 1 0.20 0 0
CUI: C1853162
Disease: Osteogenesis Imperfecta Type VII
Osteogenesis Imperfecta Type VII
1 0 1 0.20 0 0
Ehlers-Danlos syndrome, cardiac valvular form
1 0 1 0.20 0 0
CUI: C1970458
Disease: Osteogenesis imperfecta, type VIII
Osteogenesis imperfecta, type VIII
1 0 1 0.20 0 0
Ehlers-Danlos syndrome cardiac valvular type
1 0 1 0.20 0 0
CUI: C0392784
Disease: Dermatofibrosarcoma Protuberans
Dermatofibrosarcoma Protuberans
2 0 1 0.17 0 0
Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified
3 0 1 0.14 0 0
CUI: C1619692
Disease: Nephrogenic Fibrosing Dermopathy
Nephrogenic Fibrosing Dermopathy
3 0 1 0.14 0 0
EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1
3 0 1 0.14 0 0
CUI: C0002949
Disease: Aneurysm, Dissecting
Aneurysm, Dissecting
5 0 1 0.11 0 0
CUI: C0340643
Disease: Dissection of aorta
Dissection of aorta
5 0 1 0.11 0 0
CUI: C4277533
Disease: Dissection, Blood Vessel
Dissection, Blood Vessel
5 0 1 0.11 0 0
CUI: C0029172
Disease: Oral Submucous Fibrosis
Oral Submucous Fibrosis
18 0 2 9.5E-02 0 0
CUI: C0008311
Disease: Cholangitis
Cholangitis
7 0 1 9.1E-02 0 0
CUI: C1458140
Disease: Bleeding tendency
Bleeding tendency
7 0 1 9.1E-02 0 0
Autoimmune Lymphoproliferative Syndrome Type 2B
7 0 1 9.1E-02 0 0