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: C4520731
Disease: Stage II Cutaneous Melanoma AJCC v6 and v7
Stage II Cutaneous Melanoma AJCC v6 and v7 		3 0 1 0.33 0 0
CUI: C0206737
Disease: Nevus, Intradermal
Nevus, Intradermal 		4 0 1 0.25 0 0
CUI: C0268494
Disease: Oculocutaneous albinism type 1
Oculocutaneous albinism type 1 		4 2 1 0.25 1 7.1E-02
CUI: C0278880
Disease: Stage I Cutaneous Melanoma AJCC v6
Stage I Cutaneous Melanoma AJCC v6 		4 0 1 0.25 0 0
CUI: C1377589
Disease: Regressing nevus
Regressing nevus 		4 0 1 0.25 0 0
CUI: C3806221
Disease: Giant melanosomes in melanocytes
Giant melanosomes in melanocytes 		4 0 1 0.25 0 0
CUI: C4024172
Disease: Abnormality of hair pigmentation
Abnormality of hair pigmentation 		5 2 1 0.20 1 7.1E-02
CUI: C0276640
Disease: Transmissible mink encephalopathy
Transmissible mink encephalopathy 		6 0 1 0.17 0 0
CUI: C0262977
Disease: Achromia of skin
Achromia of skin 		7 0 1 0.14 0 0
CUI: C0334439
Disease: Malignant desmoplastic melanoma
Malignant desmoplastic melanoma 		7 0 1 0.14 0 0
CUI: C2676026
Disease: Optic nerve dysplasia
Optic nerve dysplasia 		7 0 1 0.14 0 0
CUI: C2931875
Disease: Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells 		9 0 1 0.11 0 0
CUI: C1864172
Disease: Peroxisome Biogenesis Disorder, Complementation Group G
Peroxisome Biogenesis Disorder, Complementation Group G 		10 0 1 1.0E-01 0 0
CUI: C0268495
Disease: Oculocutaneous albinism type 2
Oculocutaneous albinism type 2 		11 0 1 9.1E-02 0 0
CUI: C0337439
Disease: Iron measurement
Iron measurement 		12 0 1 8.3E-02 0 0
CUI: C0428578
Disease: Iron level result
Iron level result 		12 0 1 8.3E-02 0 0
CUI: C1697878
Disease: BK virus nephropathy
BK virus nephropathy 		12 0 1 8.3E-02 0 0
CUI: C0015396
Disease: Eye Color
Eye Color 		13 0 1 7.7E-02 0 0
CUI: C0035300
Disease: Abnormal retinal morphology
Abnormal retinal morphology 		13 0 1 7.7E-02 0 0
CUI: C0349515
Disease: Amelanotic Skin Melanoma
Amelanotic Skin Melanoma 		13 0 1 7.7E-02 0 0
CUI: C1328931
Disease: Multiple lentigines
Multiple lentigines 		13 0 1 7.7E-02 0 0
CUI: C1848606
Disease: Vestibular hypofunction
Vestibular hypofunction 		13 0 1 7.7E-02 0 0
CUI: C2931205
Disease: Usher syndrome, type 1A
Usher syndrome, type 1A 		14 0 1 7.1E-02 0 0
CUI: C0036651
Disease: Solar lentigo
Solar lentigo 		15 0 1 6.7E-02 0 0
CUI: C0334424
Disease: Nodular melanoma
Nodular melanoma 		15 0 1 6.7E-02 0 0