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: C0036454
Disease: Scotoma
Scotoma 		21 0 15 0.20 0 0
CUI: C1568247
Disease: Usher Syndrome, Type I
Usher Syndrome, Type I 		23 168 14 0.18 11 4.8E-02
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 16 0.18 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia 		41 0 15 0.16 0 0
CUI: C0024106
Disease: Lumpy Skin Disease
Lumpy Skin Disease 		12 0 11 0.16 0 0
CUI: C0857116
Disease: Gross obesity
Gross obesity 		12 0 11 0.16 0 0
CUI: C1840348
Disease: Hypocalciuric Hypercalcemia, Acquired
Hypocalciuric Hypercalcemia, Acquired 		13 0 11 0.16 0 0
CUI: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction 		13 0 11 0.16 0 0
CUI: C1847352
Disease: POLYMICROGYRIA, BILATERAL FRONTOPARIETAL
POLYMICROGYRIA, BILATERAL FRONTOPARIETAL 		15 0 11 0.15 0 0
CUI: C4025858
Disease: Abnormal cochlea morphology
Abnormal cochlea morphology 		16 0 11 0.15 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 14 0.15 0 0
CUI: C1568248
Disease: Usher Syndrome, Type III
Usher Syndrome, Type III 		13 24 10 0.14 1 1.0E-02
CUI: C4023018
Disease: Subcortical cerebral atrophy
Subcortical cerebral atrophy 		22 0 11 0.14 0 0
CUI: C1334386
Disease: Meningeal melanoma
Meningeal melanoma 		23 0 11 0.14 0 0
CUI: C0580174
Disease: Portal hypertensive gastropathy
Portal hypertensive gastropathy 		24 0 11 0.14 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 13 0.13 0 0
CUI: C0220659
Disease: Acrodysostosis
Acrodysostosis 		31 0 11 0.12 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 0 9 0.12 0 0
CUI: C0553665
Disease: Skin endocrine disorder
Skin endocrine disorder 		34 0 11 0.12 0 0
CUI: C0342684
Disease: Ocular albinism, type I
Ocular albinism, type I 		38 0 11 0.12 0 0
CUI: C1264039
Disease: von Willebrand Disease, Type 1
von Willebrand Disease, Type 1 		39 0 11 0.11 0 0
CUI: C0858600
Disease: Taste sweet
Taste sweet 		41 0 11 0.11 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 22 0.11 0 0
CUI: C0001916
Disease: Albinism
Albinism 		46 0 11 0.11 0 0
CUI: C1857451
Disease: Acth-Independent Macronodular Adrenal Hyperplasia
Acth-Independent Macronodular Adrenal Hyperplasia 		46 0 11 0.11 0 0