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: C1318558
Disease: Congenital melanocytic nevus
Congenital melanocytic nevus 		7 0 1 0.12 0 0
CUI: C2739810
Disease: Lentigo maligna melanoma
Lentigo maligna melanoma 		7 0 1 0.12 0 0
CUI: C0233622
Disease: Ritual compulsion
Ritual compulsion 		8 0 1 0.11 0 0
CUI: C0410533
Disease: Osteodysplasia
Osteodysplasia 		8 0 1 0.11 0 0
CUI: C0728936
Disease: Disorder of circulatory system
Disorder of circulatory system 		8 0 1 0.11 0 0
CUI: C0858864
Disease: Spot pigmented
Spot pigmented 		8 0 1 0.11 0 0
CUI: C0206735
Disease: Melanoma, Amelanotic
Melanoma, Amelanotic 		19 0 2 0.11 0 0
CUI: C4054695
Disease: Familial glucocorticoid deficiency
Familial glucocorticoid deficiency 		9 4 1 1.0E-01 1 0.17
CUI: C1298685
Disease: Chronic pain syndrome
Chronic pain syndrome 		10 0 1 9.1E-02 0 0
CUI: C0496836
Disease: Malignant tumor of eye
Malignant tumor of eye 		11 0 1 8.3E-02 0 0
CUI: C1846058
Disease: Lubs X-linked mental retardation syndrome
Lubs X-linked mental retardation syndrome 		11 0 1 8.3E-02 0 0
CUI: C1849452
Disease: SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder)
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder) 		11 13 1 8.3E-02 2 0.14
CUI: C2930995
Disease: Dyschromatosis universalis hereditaria
Dyschromatosis universalis hereditaria 		11 0 1 8.3E-02 0 0
CUI: C1862596
Disease: Familial hypobetalipoproteinemia
Familial hypobetalipoproteinemia 		12 0 1 7.7E-02 0 0
CUI: C0349515
Disease: Amelanotic Skin Melanoma
Amelanotic Skin Melanoma 		13 0 1 7.1E-02 0 0
CUI: C0858681
Disease: Vitiligo vulgaris
Vitiligo vulgaris 		13 0 1 7.1E-02 0 0
CUI: C0036651
Disease: Solar lentigo
Solar lentigo 		15 0 1 6.2E-02 0 0
CUI: C0221253
Disease: Xanthoma tendinosum
Xanthoma tendinosum 		15 0 1 6.2E-02 0 0
CUI: C0334424
Disease: Nodular melanoma
Nodular melanoma 		15 0 1 6.2E-02 0 0
CUI: C0700501
Disease: Congenital nystagmus
Congenital nystagmus 		15 0 1 6.2E-02 0 0
CUI: C0080024
Disease: Piebaldism
Piebaldism 		33 0 2 6.1E-02 0 0
CUI: C4021976
Disease: Abnormality of the lymphatic system
Abnormality of the lymphatic system 		16 0 1 5.9E-02 0 0
CUI: C0206736
Disease: Nevus, Blue
Nevus, Blue 		17 0 1 5.6E-02 0 0
CUI: C0342158
Disease: Hypothyroidism, Autoimmune
Hypothyroidism, Autoimmune 		17 0 1 5.6E-02 0 0
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 2 5.4E-02 0 0