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: C0031911
Disease: Pigmentation
Pigmentation 		1 0 1 0.50 0 0
CUI: C0342683
Disease: ALBINISM, OCULOCUTANEOUS, TYPE III
ALBINISM, OCULOCUTANEOUS, TYPE III 		1 9 1 0.50 1 9.1E-02
CUI: C2677086
Disease: Skin-Hair-Eye Pigmentation, Variation In, 11
Skin-Hair-Eye Pigmentation, Variation In, 11 		1 0 1 0.50 0 0
CUI: C2678403
Disease: UV-INDUCED SKIN DAMAGE, SUSCEPTIBILITY TO
UV-INDUCED SKIN DAMAGE, SUSCEPTIBILITY TO 		1 0 1 0.50 0 0
CUI: C2751295
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5 		1 0 1 0.50 0 0
CUI: C2751296
Disease: INCREASED ANALGESIA FROM KAPPA-OPIOID RECEPTOR AGONIST, FEMALE-SPECIFIC (disorder)
INCREASED ANALGESIA FROM KAPPA-OPIOID RECEPTOR AGONIST, FEMALE-SPECIFIC (disorder) 		1 2 1 0.50 2 0.67
CUI: C4016260
Disease: SKIN/HAIR/EYE PIGMENTATION 2, RED HAIR/FAIR SKIN
SKIN/HAIR/EYE PIGMENTATION 2, RED HAIR/FAIR SKIN 		1 3 1 0.50 2 0.50
CUI: C0022078
Disease: Iris Diseases
Iris Diseases 		2 0 1 0.33 0 0
CUI: C0240564
Disease: Pain of nose
Pain of nose 		2 0 1 0.33 0 0
CUI: C0268497
Disease: Brown oculocutaneous albinism
Brown oculocutaneous albinism 		2 0 1 0.33 0 0
CUI: C0333128
Disease: Open comedone
Open comedone 		2 0 1 0.33 0 0
CUI: C0339619
Disease: Congenital esotropia
Congenital esotropia 		2 0 1 0.33 0 0
CUI: C2931599
Disease: Oculocutaneous albinism type 3
Oculocutaneous albinism type 3 		2 0 1 0.33 0 0
CUI: C3888007
Disease: HERMANSKY-PUDLAK SYNDROME 6
HERMANSKY-PUDLAK SYNDROME 6 		2 0 1 0.33 0 0
CUI: C1304055
Disease: Brachioradial pruritus
Brachioradial pruritus 		3 0 1 0.25 0 0
CUI: C0239803
Disease: Red hair
Red hair 		9 0 2 0.22 0 0
CUI: C0040460
Disease: Toothache
Toothache 		4 0 1 0.20 0 0
CUI: C0749263
Disease: temporal pain
temporal pain 		4 0 1 0.20 0 0
CUI: C0268495
Disease: Oculocutaneous albinism type 2
Oculocutaneous albinism type 2 		11 0 2 0.18 0 0
CUI: C0265295
Disease: Jansen type metaphyseal chondrodysplasia
Jansen type metaphyseal chondrodysplasia 		5 0 1 0.17 0 0
CUI: C1842036
Disease: GIANT PIGMENTED HAIRY NEVUS
GIANT PIGMENTED HAIRY NEVUS 		5 0 1 0.17 0 0
CUI: C1859923
Disease: Freckles in sun-exposed areas
Freckles in sun-exposed areas 		5 0 1 0.17 0 0
CUI: C0233702
Disease: Algophobia
Algophobia 		6 0 1 0.14 0 0
CUI: C1860823
Disease: Trichorhinophalangeal Syndrome, Type III
Trichorhinophalangeal Syndrome, Type III 		6 0 1 0.14 0 0
CUI: C0339296
Disease: Neurotrophic keratitis
Neurotrophic keratitis 		7 0 1 0.12 0 0