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: C0546297
Disease: Hallux Varus
Hallux Varus
4 0 3 0.38 0 0
Cutis Gyrata Syndrome of Beare And Stevenson
2 0 2 0.29 0 0
CUI: C1863363
Disease: Cartilaginous trachea
Cartilaginous trachea
2 0 2 0.29 0 0
CUI: C2931888
Disease: Pfeiffer type acrocephalosyndactyly
Pfeiffer type acrocephalosyndactyly
2 0 2 0.29 0 0
CUI: C4024730
Disease: Calcaneonavicular fusion
Calcaneonavicular fusion
2 0 2 0.29 0 0
Shortening of all proximal phalanges of the fingers
2 0 2 0.29 0 0
CUI: C0409477
Disease: Ankylosis of the elbow joint
Ankylosis of the elbow joint
7 0 3 0.27 0 0
CUI: C0795998
Disease: JACKSON-WEISS SYNDROME
JACKSON-WEISS SYNDROME
3 0 2 0.25 0 0
CUI: C1864436
Disease: Muenke Syndrome
Muenke Syndrome
3 0 2 0.25 0 0
CUI: C4021723
Disease: Short middle phalanx of toe
Short middle phalanx of toe
4 0 2 0.22 0 0
CUI: C4025664
Disease: Abnormality of fibula morphology
Abnormality of fibula morphology
4 0 2 0.22 0 0
CUI: C2930865
Disease: Ramer Ladda syndrome
Ramer Ladda syndrome
10 0 3 0.21 0 0
CUI: C1275277
Disease: Soft tissue chondroma
Soft tissue chondroma
6 0 2 0.18 0 0
CUI: C1844891
Disease: Ulnar deviation of the 2nd finger
Ulnar deviation of the 2nd finger
6 0 2 0.18 0 0
CUI: C1846474
Disease: Small thenar eminence
Small thenar eminence
6 0 2 0.18 0 0
CUI: C4021164
Disease: Bicoronal synostosis
Bicoronal synostosis
6 0 2 0.18 0 0
CUI: C1842231
Disease: Broad metatarsal
Broad metatarsal
7 0 2 0.17 0 0
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome
8 0 2 0.15 0 0
CUI: C1836688
Disease: Narrow iliac wings
Narrow iliac wings
8 0 2 0.15 0 0
CUI: C1860050
Disease: Cloverleaf skull
Cloverleaf skull
8 0 2 0.15 0 0
CUI: C1865992
Disease: Short hallux
Short hallux
23 0 4 0.15 0 0
CUI: C0006262
Disease: Bronchial Fistula
Bronchial Fistula
1 0 1 0.14 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly
1 0 1 0.14 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation
1 0 1 0.14 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A
1 0 1 0.14 0 0