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: C0078917
Disease: Albinism, Ocular
Albinism, Ocular 		37 10 22 0.36 5 0.16
CUI: C0342684
Disease: Ocular albinism, type I
Ocular albinism, type I 		38 24 17 0.25 1 2.0E-02
CUI: C0024106
Disease: Lumpy Skin Disease
Lumpy Skin Disease 		12 0 11 0.23 0 0
CUI: C0857116
Disease: Gross obesity
Gross obesity 		12 0 11 0.23 0 0
CUI: C1840348
Disease: Hypocalciuric Hypercalcemia, Acquired
Hypocalciuric Hypercalcemia, Acquired 		13 0 11 0.23 0 0
CUI: C1847352
Disease: POLYMICROGYRIA, BILATERAL FRONTOPARIETAL
POLYMICROGYRIA, BILATERAL FRONTOPARIETAL 		15 0 11 0.22 0 0
CUI: C0078918
Disease: Albinism, Oculocutaneous
Albinism, Oculocutaneous 		49 45 17 0.22 6 9.1E-02
CUI: C1876214
Disease: ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT
ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT 		54 0 17 0.20 0 0
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding) 		25 4 12 0.20 3 0.11
CUI: C0032197
Disease: Platelet Storage Pool Deficiency
Platelet Storage Pool Deficiency 		22 0 11 0.19 0 0
CUI: C1334386
Disease: Meningeal melanoma
Meningeal melanoma 		23 0 11 0.19 0 0
CUI: C0580174
Disease: Portal hypertensive gastropathy
Portal hypertensive gastropathy 		24 0 11 0.19 0 0
CUI: C0079504
Disease: Hermanski-Pudlak Syndrome
Hermanski-Pudlak Syndrome 		70 0 17 0.17 0 0
CUI: C2931875
Disease: Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells 		9 0 8 0.17 0 0
CUI: C0220659
Disease: Acrodysostosis
Acrodysostosis 		31 0 11 0.17 0 0
CUI: C0151891
Disease: Retinal depigmentation
Retinal depigmentation 		19 0 9 0.16 0 0
CUI: C0553665
Disease: Skin endocrine disorder
Skin endocrine disorder 		34 0 11 0.16 0 0
CUI: C1264039
Disease: von Willebrand Disease, Type 1
von Willebrand Disease, Type 1 		39 0 11 0.15 0 0
CUI: C0858600
Disease: Taste sweet
Taste sweet 		41 0 11 0.14 0 0
CUI: C1857451
Disease: Acth-Independent Macronodular Adrenal Hyperplasia
Acth-Independent Macronodular Adrenal Hyperplasia 		46 0 11 0.14 0 0
CUI: C0005818
Disease: Blood Platelet Disorders
Blood Platelet Disorders 		59 0 12 0.13 0 0
CUI: C0162835
Disease: Hypopigmentation disorder
Hypopigmentation disorder 		126 15 19 0.12 3 7.7E-02
CUI: C0393642
Disease: Sepsis-Associated Encephalopathy
Sepsis-Associated Encephalopathy 		57 0 11 0.12 0 0
CUI: C0268495
Disease: Oculocutaneous albinism type 2
Oculocutaneous albinism type 2 		11 58 6 0.12 2 2.4E-02
CUI: C0162283
Disease: Nephrogenic Diabetes Insipidus
Nephrogenic Diabetes Insipidus 		60 0 11 0.12 0 0