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: C4048199
Disease: Ulnar deviation of the hand or of fingers of the hand
Ulnar deviation of the hand or of fingers of the hand 		11 0 6 0.35 0 0
CUI: C1860344
Disease: Hypoplastic iris stroma
Hypoplastic iris stroma 		7 0 2 0.12 0 0
CUI: C4072908
Disease: Induced vaginal delivery
Induced vaginal delivery 		10 10 2 1.0E-01 1 9.1E-02
CUI: C0231678
Disease: Ulnar deviation of the wrist
Ulnar deviation of the wrist 		14 0 2 8.3E-02 0 0
CUI: C0265729
Disease: Mesatipellic pelvis
Mesatipellic pelvis 		1 0 1 8.3E-02 0 0
CUI: C0432281
Disease: Pseudochondroplasia
Pseudochondroplasia 		1 0 1 8.3E-02 0 0
CUI: C0748397
Disease: Reynolds syndrome
Reynolds syndrome 		1 0 1 8.3E-02 0 0
CUI: C1838280
Disease: Epiphyseal dysplasia, multiple, 1
Epiphyseal dysplasia, multiple, 1 		1 0 1 8.3E-02 0 0
CUI: C1849762
Disease: Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia
Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia 		1 0 1 8.3E-02 0 0
CUI: C1852510
Disease: Craniofacial deafness hand syndrome
Craniofacial deafness hand syndrome 		1 0 1 8.3E-02 0 0
CUI: C1856637
Disease: Spatulate ribs
Spatulate ribs 		1 0 1 8.3E-02 0 0
CUI: C1859120
Disease: Anterior rib punctate calcifications
Anterior rib punctate calcifications 		1 0 1 8.3E-02 0 0
CUI: C1859121
Disease: Sternal punctate calcifications
Sternal punctate calcifications 		1 0 1 8.3E-02 0 0
CUI: C1859231
Disease: Hypoplastic olfactory lobes
Hypoplastic olfactory lobes 		1 0 1 8.3E-02 0 0
CUI: C1866048
Disease: Severe hydrops fetalis
Severe hydrops fetalis 		1 0 1 8.3E-02 0 0
CUI: C1867494
Disease: Fragmented, irregular epiphyses
Fragmented, irregular epiphyses 		1 0 1 8.3E-02 0 0
CUI: C2674705
Disease: Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy
Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy 		1 0 1 8.3E-02 0 0
CUI: C2675227
Disease: Endocrine-Cerebroosteodysplasia
Endocrine-Cerebroosteodysplasia 		1 0 1 8.3E-02 0 0
CUI: C2931461
Disease: Forney Robinson Pascoe syndrome
Forney Robinson Pascoe syndrome 		1 0 1 8.3E-02 0 0
CUI: C3179244
Disease: Pseudo Pelger-Huet Anomaly
Pseudo Pelger-Huet Anomaly 		1 0 1 8.3E-02 0 0
CUI: C3809650
Disease: BAINBRIDGE-ROPERS SYNDROME
BAINBRIDGE-ROPERS SYNDROME 		1 17 1 8.3E-02 1 5.6E-02
CUI: C4016660
Disease: EPIPHYSEAL DYSPLASIA, MULTIPLE, 1, SEVERE
EPIPHYSEAL DYSPLASIA, MULTIPLE, 1, SEVERE 		1 0 1 8.3E-02 0 0
CUI: C4021025
Disease: Synostosis of carpals/tarsals
Synostosis of carpals/tarsals 		1 0 1 8.3E-02 0 0
CUI: C4021245
Disease: Patchy variation in bone mineral density
Patchy variation in bone mineral density 		1 0 1 8.3E-02 0 0
CUI: C4021305
Disease: Small epiphyses of the phalanges of the hand
Small epiphyses of the phalanges of the hand 		1 0 1 8.3E-02 0 0