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: C3808844
Disease: OSTEOGENESIS IMPERFECTA, TYPE XV
OSTEOGENESIS IMPERFECTA, TYPE XV
1 7 1 1.00 1 0.11
CUI: C3824901
Disease: Osteoporosis in children
Osteoporosis in children
2 0 1 0.50 0 0
CUI: C0158663
Disease: Tongue absent
Tongue absent
3 0 1 0.33 0 0
CUI: C0264080
Disease: Juvenile osteoporosis
Juvenile osteoporosis
4 0 1 0.25 0 0
Bowing of limbs due to multiple fractures
4 0 1 0.25 0 0
CUI: C0012746
Disease: Dissociative disorder
Dissociative disorder
6 0 1 0.17 0 0
CUI: C3666003
Disease: Transfusion dependent anaemia
Transfusion dependent anaemia
6 0 1 0.17 0 0
CUI: C0426824
Disease: Beading of ribs
Beading of ribs
7 0 1 0.14 0 0
CUI: C0266484
Disease: Schizencephaly
Schizencephaly
10 0 1 1.0E-01 0 0
Osteogenesis imperfecta type IV (disorder)
12 0 1 8.3E-02 0 0
CUI: C1704273
Disease: Endometrial Polyp
Endometrial Polyp
16 0 1 6.2E-02 0 0
Prieto X-linked mental retardation syndrome
16 0 1 6.2E-02 0 0
CUI: C4551511
Disease: X-linked sideroblastic anemia
X-linked sideroblastic anemia
16 0 1 6.2E-02 0 0
CUI: C0079487
Disease: Helicobacter Infections
Helicobacter Infections
18 0 1 5.6E-02 0 0
Osteogenesis imperfecta type III (disorder)
18 0 1 5.6E-02 0 0
Cleft palate and bilateral cleft lip
18 0 1 5.6E-02 0 0
CUI: C0023321
Disease: Lentigo
Lentigo
19 0 1 5.3E-02 0 0
CUI: C0206674
Disease: Adenoma, Villous
Adenoma, Villous
20 0 1 5.0E-02 0 0
CUI: C0752355
Disease: Myotonia Fluctuans (disorder)
Myotonia Fluctuans (disorder)
21 0 1 4.8E-02 0 0
CUI: C4087397
Disease: Mammary gland tumor
Mammary gland tumor
22 0 1 4.5E-02 0 0
CUI: C0025218
Disease: Chloasma
Chloasma
25 0 1 4.0E-02 0 0
Compression fracture of vertebral column
25 0 1 4.0E-02 0 0
CUI: C0267111
Disease: Gastric dysplasia
Gastric dysplasia
25 0 1 4.0E-02 0 0
CUI: C1848529
Disease: Hypoplasia of the pons
Hypoplasia of the pons
30 0 1 3.3E-02 0 0
CUI: C0078981
Disease: Arachnoid Cysts
Arachnoid Cysts
31 0 1 3.2E-02 0 0