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: C0432106
Disease: Midline facial cleft - Tessier cleft 0
Midline facial cleft - Tessier cleft 0 		8 0 4 0.17 0 0
CUI: C0752355
Disease: Myotonia Fluctuans (disorder)
Myotonia Fluctuans (disorder) 		21 0 5 0.14 0 0
CUI: C0549397
Disease: Deviated nasal septum
Deviated nasal septum 		5 0 3 0.14 0 0
CUI: C1860164
Disease: Duplication of phalanx of hallux
Duplication of phalanx of hallux 		6 0 3 0.13 0 0
CUI: C4021164
Disease: Bicoronal synostosis
Bicoronal synostosis 		6 0 3 0.13 0 0
CUI: C1876203
Disease: Frontonasal dysplasia
Frontonasal dysplasia 		16 0 4 0.12 0 0
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia 		8 0 3 0.12 0 0
CUI: C1853666
Disease: Anemia, Diamond-Blackfan, 2
Anemia, Diamond-Blackfan, 2 		8 0 3 0.12 0 0
CUI: C0221363
Disease: Bifid nose
Bifid nose 		9 0 3 0.12 0 0
CUI: C1853486
Disease: Widow's peak
Widow's peak 		9 0 3 0.12 0 0
CUI: C1281931
Disease: Obstruction of nasolacrimal duct
Obstruction of nasolacrimal duct 		12 0 3 0.10 0 0
CUI: C1852464
Disease: Abnormality of the cervical spine
Abnormality of the cervical spine 		12 0 3 0.10 0 0
CUI: C1859717
Disease: Depressed nasal tip
Depressed nasal tip 		23 0 4 0.10 0 0
CUI: C0149650
Disease: Chronic mastitis
Chronic mastitis 		2 0 2 1.0E-01 0 0
CUI: C0235710
Disease: Chest discomfort
Chest discomfort 		2 0 2 1.0E-01 0 0
CUI: C0268445
Disease: Normokalemic Periodic Paralysis
Normokalemic Periodic Paralysis 		2 0 2 1.0E-01 0 0
CUI: C0340169
Disease: Simple pneumoconiosis
Simple pneumoconiosis 		2 0 2 1.0E-01 0 0
CUI: C0432124
Disease: Unicoronal craniosynostosis
Unicoronal craniosynostosis 		2 0 2 1.0E-01 0 0
CUI: C0587043
Disease: Right ventricular thrombus
Right ventricular thrombus 		2 0 2 1.0E-01 0 0
CUI: C0848538
Disease: fluid retention in lung
fluid retention in lung 		2 0 2 1.0E-01 0 0
CUI: C1333160
Disease: Lipoma of corpus callosum
Lipoma of corpus callosum 		2 0 2 1.0E-01 0 0
CUI: C1849227
Disease: Cleft of chin
Cleft of chin 		2 0 2 1.0E-01 0 0
CUI: C1863382
Disease: Absent first metatarsal
Absent first metatarsal 		2 0 2 1.0E-01 0 0
CUI: C1863389
Disease: Apert-Crouzon Disease
Apert-Crouzon Disease 		2 0 2 1.0E-01 0 0
CUI: C1865045
Disease: Symmetrical, oval parietal bone defects
Symmetrical, oval parietal bone defects 		2 0 2 1.0E-01 0 0