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: C3806218
Disease: Episodic tachypnea
Episodic tachypnea 		31 0 1 4.8E-04 0 0
CUI: C0011813
Disease: Dextrocardia
Dextrocardia 		30 0 1 4.8E-04 0 0
CUI: C1855676
Disease: Aplasia/Hypoplasia of the cerebellar vermis
Aplasia/Hypoplasia of the cerebellar vermis 		30 0 1 4.8E-04 0 0
CUI: C2677328
Disease: Cerebral hypomyelination
Cerebral hypomyelination 		29 0 1 4.8E-04 0 0
CUI: C3161174
Disease: Hemoglobin H Disease
Hemoglobin H Disease 		29 0 1 4.8E-04 0 0
CUI: C4072872
Disease: obsolete Rod-cone dystrophy
obsolete Rod-cone dystrophy 		29 0 1 4.8E-04 0 0
CUI: C0267971
Disease: Storage disease
Storage disease 		28 0 1 4.8E-04 0 0
CUI: C0269269
Disease: Inversion of nipple (disorder)
Inversion of nipple (disorder) 		27 0 1 4.8E-04 0 0
CUI: C4020730
Disease: Increased intramyocellular lipid droplets
Increased intramyocellular lipid droplets 		27 0 1 4.8E-04 0 0
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		26 0 1 4.8E-04 0 0
CUI: C0238111
Disease: Lennox-Gastaut syndrome
Lennox-Gastaut syndrome 		25 0 1 4.8E-04 0 0
CUI: C0333751
Disease: Muscle fiber atrophy
Muscle fiber atrophy 		25 0 1 4.8E-04 0 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy 		25 0 1 4.8E-04 0 0
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding) 		25 0 1 4.8E-04 0 0
CUI: C1836623
Disease: Decreased circulating cortisol level
Decreased circulating cortisol level 		23 0 1 4.8E-04 0 0
CUI: C0036454
Disease: Scotoma
Scotoma 		21 0 1 4.8E-04 0 0
CUI: C0036996
Disease: Short Rib-Polydactyly Syndrome
Short Rib-Polydactyly Syndrome 		21 0 1 4.8E-04 0 0
CUI: C0265221
Disease: Walker-Warburg congenital muscular dystrophy
Walker-Warburg congenital muscular dystrophy 		21 0 1 4.8E-04 0 0
CUI: C0311277
Disease: Obesity, Abdominal
Obesity, Abdominal 		21 0 1 4.8E-04 0 0
CUI: C0431370
Disease: Atrophy of corpus callosum
Atrophy of corpus callosum 		21 0 1 4.8E-04 0 0
CUI: C1846868
Disease: Parkinsonism with favorable response to dopaminergic medication
Parkinsonism with favorable response to dopaminergic medication 		21 0 1 4.8E-04 0 0
CUI: C1855685
Disease: Undetectable electroretinogram
Undetectable electroretinogram 		21 0 1 4.8E-04 0 0
CUI: C4024809
Disease: Chorioretinal dysplasia
Chorioretinal dysplasia 		21 0 1 4.8E-04 0 0
CUI: C0006852
Disease: Candidiasis of vagina
Candidiasis of vagina 		20 0 1 4.8E-04 0 0
CUI: C0020597
Disease: Hypobetalipoproteinemias
Hypobetalipoproteinemias 		20 0 1 4.8E-04 0 0