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: C1335684
Disease: Rectal Lipoma
Rectal Lipoma 		3 0 3 0.50 0 0
CUI: C0233593
Disease: Eye poking
Eye poking 		2 0 2 0.33 0 0
CUI: C1858080
Disease: Retinal Dystrophy, Early Onset Severe
Retinal Dystrophy, Early Onset Severe 		14 0 5 0.33 0 0
CUI: C2673929
Disease: Fundus atrophy
Fundus atrophy 		3 0 2 0.29 0 0
CUI: C3540662
Disease: Congenital Amaurosis of Retinal Origin
Congenital Amaurosis of Retinal Origin 		8 0 3 0.27 0 0
CUI: C0457193
Disease: Soft tissue mass
Soft tissue mass 		12 0 3 0.20 0 0
CUI: C3669048
Disease: Round cell tumor
Round cell tumor 		12 0 3 0.20 0 0
CUI: C0234362
Disease: Synkinesis
Synkinesis 		13 0 3 0.19 0 0
CUI: C0344297
Disease: Choroidal sclerosis
Choroidal sclerosis 		1 0 1 0.17 0 0
CUI: C1333044
Disease: Chronic Myelomonocytic Leukemia-2
Chronic Myelomonocytic Leukemia-2 		1 0 1 0.17 0 0
CUI: C1833564
Disease: CONE-ROD DYSTROPHY 1 (disorder)
CONE-ROD DYSTROPHY 1 (disorder) 		1 0 1 0.17 0 0
CUI: C1835407
Disease: HEPATITIS C VIRUS, SUSCEPTIBILITY TO
HEPATITIS C VIRUS, SUSCEPTIBILITY TO 		1 0 1 0.17 0 0
CUI: C1839025
Disease: Decreased light- and dark-adapted electroretinogram amplitude
Decreased light- and dark-adapted electroretinogram amplitude 		15 0 3 0.17 0 0
CUI: C2673931
Disease: Hyperthreoninuria
Hyperthreoninuria 		1 0 1 0.17 0 0
CUI: C2750063
Disease: Leber Congenital Amaurosis 14
Leber Congenital Amaurosis 14 		1 0 1 0.17 0 0
CUI: C2750064
Disease: Retinal Dystrophy, Early-Onset Severe, Lrat-Related
Retinal Dystrophy, Early-Onset Severe, Lrat-Related 		1 0 1 0.17 0 0
CUI: C2750065
Disease: RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED
RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED 		1 0 1 0.17 0 0
CUI: C3151086
Disease: Retinitis Pigmentosa 20
Retinitis Pigmentosa 20 		1 0 1 0.17 0 0
CUI: C4274354
Disease: Severe early childhood onset retinal dystrophy
Severe early childhood onset retinal dystrophy 		1 0 1 0.17 0 0
CUI: C4551884
Disease: Choroidal Dystrophy, Central Areolar 1
Choroidal Dystrophy, Central Areolar 1 		1 0 1 0.17 0 0
CUI: C4707246
Disease: Biallelic RPE65 mutation associated retinal dystrophy
Biallelic RPE65 mutation associated retinal dystrophy 		1 0 1 0.17 0 0
CUI: C0005754
Disease: Congenital blindness
Congenital blindness 		16 0 3 0.16 0 0
CUI: C0015398
Disease: Eye Diseases, Hereditary
Eye Diseases, Hereditary 		9 0 2 0.15 0 0
CUI: C1848861
Disease: Hyperthreoninemia
Hyperthreoninemia 		2 0 1 0.14 0 0
CUI: C3808249
Disease: Abnormality of the optic disc
Abnormality of the optic disc 		26 0 4 0.14 0 0