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: C1855331
Disease: Olfactory lobe agenesis
Olfactory lobe agenesis 		7 0 1 0.12 0 0
CUI: C1860339
Disease: WAARDENBURG SYNDROME, TYPE IIA
WAARDENBURG SYNDROME, TYPE IIA 		7 0 1 0.12 0 0
CUI: C1860344
Disease: Hypoplastic iris stroma
Hypoplastic iris stroma 		7 0 1 0.12 0 0
CUI: C1836736
Disease: White eyelashes
White eyelashes 		8 0 1 0.11 0 0
CUI: C0151891
Disease: Retinal depigmentation
Retinal depigmentation 		19 0 2 0.11 0 0
CUI: C0206735
Disease: Melanoma, Amelanotic
Melanoma, Amelanotic 		19 0 2 0.11 0 0
CUI: C2700265
Disease: Waardenburg Syndrome Type 2
Waardenburg Syndrome Type 2 		9 0 1 1.0E-01 0 0
CUI: C2931875
Disease: Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells 		9 0 1 1.0E-01 0 0
CUI: C1704421
Disease: Skin Pigmentation Disorder
Skin Pigmentation Disorder 		21 0 2 9.5E-02 0 0
CUI: C3266898
Disease: Waardenburg Syndrome
Waardenburg Syndrome 		21 0 2 9.5E-02 0 0
CUI: C1864172
Disease: Peroxisome Biogenesis Disorder, Complementation Group G
Peroxisome Biogenesis Disorder, Complementation Group G 		10 0 1 9.1E-02 0 0
CUI: C3278401
Disease: Hypopigmentation of hair
Hypopigmentation of hair 		23 0 2 8.7E-02 0 0
CUI: C0268495
Disease: Oculocutaneous albinism type 2
Oculocutaneous albinism type 2 		11 0 1 8.3E-02 0 0
CUI: C0025218
Disease: Chloasma
Chloasma 		25 0 2 8.0E-02 0 0
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding) 		25 0 2 8.0E-02 0 0
CUI: C0337439
Disease: Iron measurement
Iron measurement 		12 0 1 7.7E-02 0 0
CUI: C0344312
Disease: White forelock
White forelock 		12 0 1 7.7E-02 0 0
CUI: C0428578
Disease: Iron level result
Iron level result 		12 0 1 7.7E-02 0 0
CUI: C1697878
Disease: BK virus nephropathy
BK virus nephropathy 		12 0 1 7.7E-02 0 0
CUI: C1836806
Disease: Mild microcephaly
Mild microcephaly 		12 0 1 7.7E-02 0 0
CUI: C1848519
Disease: WAARDENBURG SYNDROME, TYPE 4A
WAARDENBURG SYNDROME, TYPE 4A 		12 0 1 7.7E-02 0 0
CUI: C0346053
Disease: Atypical fibroxanthoma of skin
Atypical fibroxanthoma of skin 		27 0 2 7.4E-02 0 0
CUI: C0015396
Disease: Eye Color
Eye Color 		13 0 1 7.1E-02 0 0
CUI: C0035300
Disease: Abnormal retinal morphology
Abnormal retinal morphology 		13 0 1 7.1E-02 0 0
CUI: C0349515
Disease: Amelanotic Skin Melanoma
Amelanotic Skin Melanoma 		13 0 1 7.1E-02 0 0