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: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 8.3E-02 0 0
CUI: C0232193
Disease: Rhythm from artificial pacing
Rhythm from artificial pacing 		1 0 1 8.3E-02 0 0
CUI: C0266445
Disease: Congenital atresia of vas deferens
Congenital atresia of vas deferens 		1 0 1 8.3E-02 0 0
CUI: C0345286
Disease: Abnormal liver lobulation
Abnormal liver lobulation 		1 0 1 8.3E-02 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis 		1 0 1 8.3E-02 0 0
CUI: C0859055
Disease: Oedema vascular
Oedema vascular 		1 0 1 8.3E-02 0 0
CUI: C1300256
Disease: Thanatophoric dysplasia, type 1
Thanatophoric dysplasia, type 1 		1 0 1 8.3E-02 0 0
CUI: C1567427
Disease: Bilateral Multicystic Dysplastic Kidneys
Bilateral Multicystic Dysplastic Kidneys 		1 0 1 8.3E-02 0 0
CUI: C1833563
Disease: Cleft Lip, Congenital Healed
Cleft Lip, Congenital Healed 		1 0 1 8.3E-02 0 0
CUI: C1833999
Disease: Retinal pigmentary degeneration
Retinal pigmentary degeneration 		1 0 1 8.3E-02 0 0
CUI: C1842691
Disease: Diaphanospondylodysostosis
Diaphanospondylodysostosis 		1 0 1 8.3E-02 0 0
CUI: C1842695
Disease: Absent in utero rib ossification
Absent in utero rib ossification 		1 0 1 8.3E-02 0 0
CUI: C1842698
Disease: Absent in utero ossification of vertebral bodies
Absent in utero ossification of vertebral bodies 		1 0 1 8.3E-02 0 0
CUI: C1851152
Disease: SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS
SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS 		1 0 1 8.3E-02 0 0
CUI: C1857780
Disease: JOUBERT SYNDROME 5
JOUBERT SYNDROME 5 		1 45 1 8.3E-02 1 2.1E-02
CUI: C1857821
Disease: LEBER CONGENITAL AMAUROSIS 10 (disorder)
LEBER CONGENITAL AMAUROSIS 10 (disorder) 		1 17 1 8.3E-02 1 5.0E-02
CUI: C1861213
Disease: Wide-cupped costochondral junctions
Wide-cupped costochondral junctions 		1 0 1 8.3E-02 0 0
CUI: C1863423
Disease: Lumbar kyphosis in infancy
Lumbar kyphosis in infancy 		1 0 1 8.3E-02 0 0
CUI: C1864689
Disease: MICROPHTHALMIA, SYNDROMIC 6 (disorder)
MICROPHTHALMIA, SYNDROMIC 6 (disorder) 		1 0 1 8.3E-02 0 0
CUI: C1864825
Disease: Frias syndrome
Frias syndrome 		1 0 1 8.3E-02 0 0
CUI: C1864852
Disease: CATSHL syndrome
CATSHL syndrome 		1 0 1 8.3E-02 0 0
CUI: C1864854
Disease: Broad femoral metaphyses
Broad femoral metaphyses 		1 0 1 8.3E-02 0 0
CUI: C1970161
Disease: MECKEL SYNDROME, TYPE 4
MECKEL SYNDROME, TYPE 4 		1 26 1 8.3E-02 1 3.4E-02
CUI: C2674171
Disease: Lethal short-limbed short stature
Lethal short-limbed short stature 		1 0 1 8.3E-02 0 0
CUI: C2675562
Disease: Unossified sacrum
Unossified sacrum 		1 0 1 8.3E-02 0 0