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: C0265695
Disease: Congenital fusion of ribs
Congenital fusion of ribs 		37 0 15 0.17 0 0
CUI: C1840380
Disease: Persistent cavum septum pellucidum
Persistent cavum septum pellucidum 		17 0 8 0.11 0 0
CUI: C0265677
Disease: Congenital hemivertebra
Congenital hemivertebra 		49 0 11 0.10 0 0
CUI: C1860816
Disease: Preauricular skin tag
Preauricular skin tag 		53 0 11 0.10 0 0
CUI: C1844825
Disease: Hyperconvex fingernails
Hyperconvex fingernails 		12 0 7 9.7E-02 0 0
CUI: C0575157
Disease: Deformity of spine
Deformity of spine 		58 0 11 9.6E-02 0 0
CUI: C1855728
Disease: Low posterior hairline
Low posterior hairline 		86 0 13 9.3E-02 0 0
CUI: C0266610
Disease: Preauricular dimple
Preauricular dimple 		40 0 9 9.2E-02 0 0
CUI: C2919828
Disease: Chronic ulcerative colitis
Chronic ulcerative colitis 		40 0 9 9.2E-02 0 0
CUI: C1860243
Disease: Abnormal sternal ossification
Abnormal sternal ossification 		6 0 6 9.0E-02 0 0
CUI: C1860244
Disease: Malrotation of small bowel
Malrotation of small bowel 		7 0 6 8.8E-02 0 0
CUI: C0796117
Disease: Pitt-Rogers-Danks Syndrome
Pitt-Rogers-Danks Syndrome 		8 0 6 8.7E-02 0 0
CUI: C1839858
Disease: Periventricular cysts
Periventricular cysts 		9 0 6 8.6E-02 0 0
CUI: C1860253
Disease: Pseudoepiphyses of the metacarpals
Pseudoepiphyses of the metacarpals 		9 0 6 8.6E-02 0 0
CUI: C0265341
Disease: Rieger syndrome
Rieger syndrome 		23 0 7 8.4E-02 0 0
CUI: C1865992
Disease: Short hallux
Short hallux 		23 0 7 8.4E-02 0 0
CUI: C0271240
Disease: Blindness of one eye (disorder)
Blindness of one eye (disorder) 		11 0 6 8.3E-02 0 0
CUI: C0345397
Disease: Accessory rib
Accessory rib 		12 0 6 8.2E-02 0 0
CUI: C0701818
Disease: Choledocholithiasis
Choledocholithiasis 		12 0 6 8.2E-02 0 0
CUI: C1848977
Disease: Short upper lip
Short upper lip 		12 0 6 8.2E-02 0 0
CUI: C1968999
Disease: Rib segmentation abnormalities
Rib segmentation abnormalities 		12 0 6 8.2E-02 0 0
CUI: C3495489
Disease: Rieger eye malformation sequence
Rieger eye malformation sequence 		13 0 6 8.1E-02 0 0
CUI: C0432163
Disease: Defect of vertebral segmentation
Defect of vertebral segmentation 		40 0 8 8.1E-02 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 8 8.0E-02 0 0
CUI: C1271219
Disease: Congenital ectopic pupil
Congenital ectopic pupil 		14 0 6 8.0E-02 0 0