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: C0339284
Disease: Polymorphous corneal dystrophy
Polymorphous corneal dystrophy 		14 0 7 5.8E-02 0 0
CUI: C1858679
Disease: CATARACT, AUTOSOMAL DOMINANT
CATARACT, AUTOSOMAL DOMINANT 		14 0 7 5.8E-02 0 0
CUI: C0009691
Disease: Congenital cataract
Congenital cataract 		105 0 12 5.8E-02 0 0
CUI: C0266544
Disease: Microcornea
Microcornea 		129 0 13 5.7E-02 0 0
CUI: C4022989
Disease: Absent outer dynein arms
Absent outer dynein arms 		6 0 6 5.3E-02 0 0
CUI: C0344530
Disease: Congenital keratoglobus
Congenital keratoglobus 		46 0 8 5.3E-02 0 0
CUI: C0521707
Disease: Bilateral cataracts (disorder)
Bilateral cataracts (disorder) 		166 0 14 5.3E-02 0 0
CUI: C0266551
Disease: Congenital coloboma of iris
Congenital coloboma of iris 		148 0 13 5.2E-02 0 0
CUI: C0022578
Disease: Keratoconus
Keratoconus 		269 0 19 5.2E-02 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 7 5.2E-02 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 7 5.2E-02 0 0
CUI: C4022983
Disease: Abnormal ciliary motility
Abnormal ciliary motility 		9 0 6 5.2E-02 0 0
CUI: C0265998
Disease: ANONYCHIA
ANONYCHIA 		30 0 7 5.1E-02 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 7 5.1E-02 0 0
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		30 0 7 5.1E-02 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 7 5.1E-02 0 0
CUI: C0240063
Disease: Coloboma of iris
Coloboma of iris 		153 0 13 5.1E-02 0 0
CUI: C1275685
Disease: Avellino corneal dystrophy
Avellino corneal dystrophy 		115 14 11 5.1E-02 8 0.26
CUI: C0027092
Disease: Myopia
Myopia 		490 0 29 5.1E-02 0 0
CUI: C0032285
Disease: Pneumonia
Pneumonia 		1032 0 55 5.0E-02 0 0
CUI: C1833118
Disease: Cataract, Pulverulent
Cataract, Pulverulent 		12 0 6 5.0E-02 0 0
CUI: C0221260
Disease: Dystrophia unguium
Dystrophia unguium 		81 0 9 4.9E-02 0 0
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		39 0 7 4.8E-02 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 7 4.8E-02 0 0
CUI: C1852438
Disease: CATARACT, COPPOCK-LIKE
CATARACT, COPPOCK-LIKE 		20 0 6 4.7E-02 0 0