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: C0153536
Disease: Malignant melanoma of skin of lower limb
Malignant melanoma of skin of lower limb 		32 42 32 1.00 42 1.00
CUI: C0406208
Disease: Suntan
Suntan 		53 94 7 9.0E-02 2 1.5E-02
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		507 248 32 6.3E-02 42 0.17
CUI: C0268503
Disease: Autosomal recessive ocular albinism
Autosomal recessive ocular albinism 		2 0 2 6.2E-02 0 0
CUI: C1865427
Disease: GLAUCOMA 1, OPEN ANGLE, D (disorder)
GLAUCOMA 1, OPEN ANGLE, D (disorder) 		2 0 2 6.2E-02 0 0
CUI: C1876175
Disease: Ataxia-Telangiectasia Variant
Ataxia-Telangiectasia Variant 		2 0 2 6.2E-02 0 0
CUI: C4017102
Disease: ATAXIA-TELANGIECTASIA WITHOUT IMMUNODEFICIENCY
ATAXIA-TELANGIECTASIA WITHOUT IMMUNODEFICIENCY 		2 0 2 6.2E-02 0 0
CUI: C4310623
Disease: ANTERIOR SEGMENT DYSGENESIS 6
ANTERIOR SEGMENT DYSGENESIS 6 		2 0 2 6.2E-02 0 0
CUI: C0311251
Disease: Simple buphthalmos
Simple buphthalmos 		3 0 2 6.1E-02 0 0
CUI: C1856439
Disease: GLAUCOMA 3, PRIMARY CONGENITAL, A
GLAUCOMA 3, PRIMARY CONGENITAL, A 		3 0 2 6.1E-02 0 0
CUI: C3547187
Disease: response to metformin
response to metformin 		3 0 2 6.1E-02 0 0
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		58 0 5 5.9E-02 0 0
CUI: C0206737
Disease: Nevus, Intradermal
Nevus, Intradermal 		4 0 2 5.9E-02 0 0
CUI: C1832977
Disease: GLAUCOMA 3, PRIMARY INFANTILE, B
GLAUCOMA 3, PRIMARY INFANTILE, B 		4 0 2 5.9E-02 0 0
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		24 0 3 5.7E-02 0 0
CUI: C0029440
Disease: Osteoma
Osteoma 		6 0 2 5.6E-02 0 0
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		64 0 5 5.5E-02 0 0
CUI: C0025209
Disease: Melanosis
Melanosis 		26 0 3 5.5E-02 0 0
CUI: C0276041
Disease: Chronic respiratory disease due to Mycoplasma gallisepticum
Chronic respiratory disease due to Mycoplasma gallisepticum 		7 0 2 5.4E-02 0 0
CUI: C4310809
Disease: ANTERIOR SEGMENT DYSGENESIS 5
ANTERIOR SEGMENT DYSGENESIS 5 		7 0 2 5.4E-02 0 0
CUI: C0018498
Disease: Hair Color
Hair Color 		130 312 8 5.2E-02 1 2.8E-03
CUI: C2931875
Disease: Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells 		9 0 2 5.1E-02 0 0
CUI: C0268495
Disease: Oculocutaneous albinism type 2
Oculocutaneous albinism type 2 		11 0 2 4.9E-02 0 0
CUI: C3469522
Disease: BREAST CANCER, SUSCEPTIBILITY TO
BREAST CANCER, SUSCEPTIBILITY TO 		11 0 2 4.9E-02 0 0
CUI: C1697878
Disease: BK virus nephropathy
BK virus nephropathy 		12 0 2 4.8E-02 0 0