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: C4021723
Disease: Short middle phalanx of toe
Short middle phalanx of toe 		4 0 2 8.7E-02 0 0
CUI: C1854520
Disease: SEBASTIAN SYNDROME
SEBASTIAN SYNDROME 		42 0 5 8.6E-02 0 0
CUI: C4700085
Disease: Chronic wasting disease (CWD)
Chronic wasting disease (CWD) 		5 0 2 8.3E-02 0 0
CUI: C1275277
Disease: Soft tissue chondroma
Soft tissue chondroma 		6 0 2 8.0E-02 0 0
CUI: C1866260
Disease: Peroxisome Biogenesis Disorder, Complementation Group H
Peroxisome Biogenesis Disorder, Complementation Group H 		6 0 2 8.0E-02 0 0
CUI: C4021164
Disease: Bicoronal synostosis
Bicoronal synostosis 		6 0 2 8.0E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 3 7.9E-02 0 0
CUI: C0409477
Disease: Ankylosis of the elbow joint
Ankylosis of the elbow joint 		7 0 2 7.7E-02 0 0
CUI: C1842231
Disease: Broad metatarsal
Broad metatarsal 		7 0 2 7.7E-02 0 0
CUI: C1856912
Disease: Shortening of all middle phalanges of the fingers
Shortening of all middle phalanges of the fingers 		7 0 2 7.7E-02 0 0
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		8 0 2 7.4E-02 0 0
CUI: C1860050
Disease: Cloverleaf skull
Cloverleaf skull 		8 0 2 7.4E-02 0 0
CUI: C0085637
Disease: Oculogyric crisis
Oculogyric crisis 		9 0 2 7.1E-02 0 0
CUI: C0238378
Disease: Desquamative interstitial pneumonia
Desquamative interstitial pneumonia 		9 0 2 7.1E-02 0 0
CUI: C0263912
Disease: Rotator cuff syndrome
Rotator cuff syndrome 		54 0 5 7.1E-02 0 0
CUI: C1399930
Disease: Attention deficit-hyperactivity
Attention deficit-hyperactivity 		9 0 2 7.1E-02 0 0
CUI: C1857484
Disease: Brachyturricephaly
Brachyturricephaly 		9 0 2 7.1E-02 0 0
CUI: C4694057
Disease: Taq1A POLYMORPHISM
Taq1A POLYMORPHISM 		9 0 2 7.1E-02 0 0
CUI: C0017495
Disease: Gerstmann-Straussler-Scheinker Disease
Gerstmann-Straussler-Scheinker Disease 		56 0 5 6.9E-02 0 0
CUI: C0264353
Disease: Bronchomalacia
Bronchomalacia 		10 0 2 6.9E-02 0 0
CUI: C2930865
Disease: Ramer Ladda syndrome
Ramer Ladda syndrome 		10 0 2 6.9E-02 0 0
CUI: C4025750
Disease: Abnormality of the nasopharynx
Abnormality of the nasopharynx 		10 0 2 6.9E-02 0 0
CUI: C1852467
Disease: Creutzfeldt-Jakob Disease, Sporadic
Creutzfeldt-Jakob Disease, Sporadic 		57 0 5 6.8E-02 0 0
CUI: C0262376
Disease: anxiety generalized
anxiety generalized 		11 0 2 6.7E-02 0 0
CUI: C0346053
Disease: Atypical fibroxanthoma of skin
Atypical fibroxanthoma of skin 		27 0 3 6.7E-02 0 0