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: C0221391
Disease: Melanosis coli
Melanosis coli 		22 5 15 0.45 5 0.22
CUI: C1318558
Disease: Congenital melanocytic nevus
Congenital melanocytic nevus 		7 0 4 0.14 0 0
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		24 72 6 0.14 6 6.7E-02
CUI: C0016689
Disease: Freckles
Freckles 		45 10 8 0.13 7 0.27
CUI: C0334424
Disease: Nodular melanoma
Nodular melanoma 		15 0 4 0.11 0 0
CUI: C1334240
Disease: Intracranial Germinoma
Intracranial Germinoma 		6 0 3 0.10 0 0
CUI: C0206736
Disease: Nevus, Blue
Nevus, Blue 		17 0 4 0.10 0 0
CUI: C0334439
Disease: Malignant desmoplastic melanoma
Malignant desmoplastic melanoma 		7 0 3 1.0E-01 0 0
CUI: C2739810
Disease: Lentigo maligna melanoma
Lentigo maligna melanoma 		7 0 3 1.0E-01 0 0
CUI: C4725861
Disease: Metastatic Malignant Neoplasm in the Viscera
Metastatic Malignant Neoplasm in the Viscera 		30 0 5 9.8E-02 0 0
CUI: C0023321
Disease: Lentigo
Lentigo 		19 0 4 9.8E-02 0 0
CUI: C0406208
Disease: Suntan
Suntan 		53 94 7 9.7E-02 3 2.6E-02
CUI: C0858864
Disease: Spot pigmented
Spot pigmented 		8 0 3 9.7E-02 0 0
CUI: C1455705
Disease: Pulmonary Histiocytosis X
Pulmonary Histiocytosis X 		9 0 3 9.4E-02 0 0
CUI: C0021432
Disease: Infratentorial Neoplasms
Infratentorial Neoplasms 		11 0 3 8.8E-02 0 0
CUI: C0268495
Disease: Oculocutaneous albinism type 2
Oculocutaneous albinism type 2 		11 0 3 8.8E-02 0 0
CUI: C1849452
Disease: SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder)
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder) 		11 13 3 8.8E-02 1 2.9E-02
CUI: C0153687
Disease: Secondary malignant neoplasm of skin
Secondary malignant neoplasm of skin 		37 0 5 8.6E-02 0 0
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding) 		25 0 4 8.5E-02 0 0
CUI: C0015396
Disease: Eye Color
Eye Color 		13 31 3 8.3E-02 1 1.9E-02
CUI: C0349515
Disease: Amelanotic Skin Melanoma
Amelanotic Skin Melanoma 		13 0 3 8.3E-02 0 0
CUI: C4287590
Disease: Thyroid Gland Noninvasive Follicular Neoplasm with Papillary-Like Nuclear Features
Thyroid Gland Noninvasive Follicular Neoplasm with Papillary-Like Nuclear Features 		13 0 3 8.3E-02 0 0
CUI: C0220654
Disease: Meningeal Carcinomatosis
Meningeal Carcinomatosis 		14 0 3 8.1E-02 0 0
CUI: C1333992
Disease: Hereditary Ovarian Carcinoma
Hereditary Ovarian Carcinoma 		14 0 3 8.1E-02 0 0
CUI: C0746408
Disease: mass lesion
mass lesion 		15 0 3 7.9E-02 0 0