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: C1846460
Disease: Abnormality of the outer ear
Abnormality of the outer ear 		95 0 1 2.2E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 4 1 2.2E-03 2 5.7E-02
CUI: C1844704
Disease: Platyspondyly
Platyspondyly 		93 0 1 2.2E-03 0 0
CUI: C0423112
Disease: Short palpebral fissure
Short palpebral fissure 		91 0 1 2.3E-03 0 0
CUI: C1837463
Disease: Narrow face
Narrow face 		87 0 1 2.3E-03 0 0
CUI: C0339525
Disease: Autosomal dominant retinitis pigmentosa
Autosomal dominant retinitis pigmentosa 		85 0 1 2.3E-03 0 0
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele 		85 0 1 2.3E-03 0 0
CUI: C3806467
Disease: Respiratory insufficiency due to muscle weakness
Respiratory insufficiency due to muscle weakness 		85 0 1 2.3E-03 0 0
CUI: C0424731
Disease: Single transverse palmar crease
Single transverse palmar crease 		78 0 1 2.3E-03 0 0
CUI: C0241726
Disease: Delayed ability to walk
Delayed ability to walk 		77 0 1 2.3E-03 0 0
CUI: C0158733
Disease: Hand polydactyly
Hand polydactyly 		75 0 1 2.3E-03 0 0
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		75 0 1 2.3E-03 0 0
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia 		75 0 1 2.3E-03 0 0
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver 		75 0 1 2.3E-03 0 0
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure) 		74 0 1 2.3E-03 0 0
CUI: C4023106
Disease: Obstructive azoospermia
Obstructive azoospermia 		74 0 1 2.3E-03 0 0
CUI: C1842366
Disease: Low anterior hairline
Low anterior hairline 		71 0 1 2.4E-03 0 0
CUI: C1866134
Disease: Wide anterior fontanel
Wide anterior fontanel 		71 0 1 2.4E-03 0 0
CUI: C0426415
Disease: Large nose
Large nose 		70 0 1 2.4E-03 0 0
CUI: C0020678
Disease: Hypotrichosis
Hypotrichosis 		69 0 1 2.4E-03 0 0
CUI: C0240538
Disease: Convex nasal ridge
Convex nasal ridge 		69 0 1 2.4E-03 0 0
CUI: C1842083
Disease: Abnormality of the ribs
Abnormality of the ribs 		69 0 1 2.4E-03 0 0
CUI: C4282407
Disease: Sparse and thin eyebrow
Sparse and thin eyebrow 		68 0 1 2.4E-03 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 1 2.4E-03 0 0
CUI: C3501844
Disease: Familial Nonmedullary Thyroid Cancer
Familial Nonmedullary Thyroid Cancer 		66 0 1 2.4E-03 0 0