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: C0149771
Disease: Rectocele
Rectocele 		1 0 1 1.00 0 0
CUI: C0730366
Disease: Rod dystrophy
Rod dystrophy 		2 0 1 0.50 0 0
CUI: C4288779
Disease: Major Congenital Anomaly
Major Congenital Anomaly 		2 0 1 0.50 0 0
CUI: C3161220
Disease: Tuberculin (skin test) positive
Tuberculin (skin test) positive 		3 0 1 0.33 0 0
CUI: C4509881
Disease: Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus
Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus 		3 0 1 0.33 0 0
CUI: C0339513
Disease: Dominant drusen
Dominant drusen 		4 0 1 0.25 0 0
CUI: C1320640
Disease: Peripheral retinal degeneration
Peripheral retinal degeneration 		4 0 1 0.25 0 0
CUI: C4024762
Disease: Pattern dystrophy of the retina
Pattern dystrophy of the retina 		4 0 1 0.25 0 0
CUI: C0158940
Disease: Transitory tachypnea of newborn
Transitory tachypnea of newborn 		5 0 1 0.20 0 0
CUI: C1842475
Disease: Retinitis Pigmentosa 7
Retinitis Pigmentosa 7 		7 0 1 0.14 0 0
CUI: C4511237
Disease: Butterfly-shaped pigmentary macular dystrophy
Butterfly-shaped pigmentary macular dystrophy 		7 0 1 0.14 0 0
CUI: C1842914
Disease: Adult-Onset Vitelliform Macular Dystrophy
Adult-Onset Vitelliform Macular Dystrophy 		8 0 1 0.12 0 0
CUI: C3831078
Disease: Clinical Chorioamnionitis
Clinical Chorioamnionitis 		8 0 1 0.12 0 0
CUI: C1405854
Disease: Retinitis punctata albescens (disorder)
Retinitis punctata albescens (disorder) 		10 0 1 1.0E-01 0 0
CUI: C1536451
Disease: Central areolar choroidal sclerosis
Central areolar choroidal sclerosis 		10 0 1 1.0E-01 0 0
CUI: C3711368
Disease: Surfactant Dysfunction
Surfactant Dysfunction 		10 0 1 1.0E-01 0 0
CUI: C0456065
Disease: Infant, Extremely Low Birth Weight
Infant, Extremely Low Birth Weight 		15 0 1 6.7E-02 0 0
CUI: C1855465
Disease: STARGARDT DISEASE 1 (disorder)
STARGARDT DISEASE 1 (disorder) 		23 0 1 4.3E-02 0 0
CUI: C3714602
Disease: Staphylococcal toxic shock syndrome
Staphylococcal toxic shock syndrome 		28 0 1 3.6E-02 0 0
CUI: C0339508
Disease: Hereditary macular dystrophy
Hereditary macular dystrophy 		39 0 1 2.6E-02 0 0
CUI: C0007370
Disease: Catalepsy
Catalepsy 		43 0 1 2.3E-02 0 0
CUI: C0024437
Disease: Macular degeneration
Macular degeneration 		44 0 1 2.3E-02 0 0
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease 		45 0 1 2.2E-02 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 1 2.1E-02 0 0
CUI: C0272170
Disease: Shwachman syndrome
Shwachman syndrome 		49 0 1 2.0E-02 0 0