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: C0578626
Disease: blue iris (physical finding)
blue iris (physical finding) 		28 0 8 0.21 0 0
CUI: C1848519
Disease: WAARDENBURG SYNDROME, TYPE 4A
WAARDENBURG SYNDROME, TYPE 4A 		12 0 5 0.19 0 0
CUI: C1836737
Disease: White eyebrow
White eyebrow 		7 0 4 0.18 0 0
CUI: C1836736
Disease: White eyelashes
White eyelashes 		8 0 4 0.17 0 0
CUI: C2700265
Disease: Waardenburg Syndrome Type 2
Waardenburg Syndrome Type 2 		9 0 4 0.17 0 0
CUI: C0423318
Disease: Heterochromia iridis
Heterochromia iridis 		17 10 5 0.16 1 7.1E-02
CUI: C0001916
Disease: Albinism
Albinism 		46 0 9 0.16 0 0
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding) 		25 0 6 0.16 0 0
CUI: C4316813
Disease: Dystopia canthorum
Dystopia canthorum 		3 0 3 0.16 0 0
CUI: C0268495
Disease: Oculocutaneous albinism type 2
Oculocutaneous albinism type 2 		11 0 4 0.15 0 0
CUI: C0344312
Disease: White forelock
White forelock 		12 0 4 0.15 0 0
CUI: C3266898
Disease: Waardenburg Syndrome
Waardenburg Syndrome 		21 0 5 0.14 0 0
CUI: C3278401
Disease: Hypopigmentation of hair
Hypopigmentation of hair 		23 0 5 0.14 0 0
CUI: C1855331
Disease: Olfactory lobe agenesis
Olfactory lobe agenesis 		7 0 3 0.13 0 0
CUI: C1860339
Disease: WAARDENBURG SYNDROME, TYPE IIA
WAARDENBURG SYNDROME, TYPE IIA 		7 0 3 0.13 0 0
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1 		16 0 4 0.13 0 0
CUI: C0029131
Disease: Abnormality of the optic nerve
Abnormality of the optic nerve 		18 0 4 0.12 0 0
CUI: C0078917
Disease: Albinism, Ocular
Albinism, Ocular 		37 0 6 0.12 0 0
CUI: C2931875
Disease: Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells 		9 0 3 0.12 0 0
CUI: C1704421
Disease: Skin Pigmentation Disorder
Skin Pigmentation Disorder 		21 0 4 0.11 0 0
CUI: C0080024
Disease: Piebaldism
Piebaldism 		33 0 5 0.11 0 0
CUI: C0263498
Disease: Premature canities
Premature canities 		33 4 5 0.11 1 0.12
CUI: C1876214
Disease: ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT
ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT 		54 0 7 0.11 0 0
CUI: C0078921
Disease: Albinism, Tyrosinase-Negative
Albinism, Tyrosinase-Negative 		2 0 2 0.11 0 0
CUI: C0078922
Disease: Albinism, Tyrosinase-Positive
Albinism, Tyrosinase-Positive 		2 0 2 0.11 0 0