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: C0078921
Disease: Albinism, Tyrosinase-Negative
Albinism, Tyrosinase-Negative 		2 0 2 1.00 0 0
CUI: C0078922
Disease: Albinism, Tyrosinase-Positive
Albinism, Tyrosinase-Positive 		2 0 2 1.00 0 0
CUI: C0078923
Disease: Albinism, Yellow-Mutant
Albinism, Yellow-Mutant 		2 0 2 1.00 0 0
CUI: C3152204
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8 		2 2 2 1.00 1 6.7E-02
CUI: C4525234
Disease: Xiphophorus Melanoma
Xiphophorus Melanoma 		2 0 2 1.00 0 0
CUI: C1845069
Disease: ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder)
ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder) 		3 2 2 0.67 2 0.14
CUI: C0268500
Disease: Yellow mutant oculocutaneous albinism
Yellow mutant oculocutaneous albinism 		1 2 1 0.50 1 6.7E-02
CUI: C0333008
Disease: Congenital hypopigmentation
Congenital hypopigmentation 		1 0 1 0.50 0 0
CUI: C0346977
Disease: Secondary malignant neoplasm of spleen
Secondary malignant neoplasm of spleen 		1 0 1 0.50 0 0
CUI: C0391816
Disease: Tietz syndrome
Tietz syndrome 		1 0 1 0.50 0 0
CUI: C1313983
Disease: Acute contagious conjunctivitis
Acute contagious conjunctivitis 		1 0 1 0.50 0 0
CUI: C1847024
Disease: ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder)
ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder) 		1 24 1 0.50 13 0.52
CUI: C1847132
Disease: ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE
ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE 		1 2 1 0.50 1 6.7E-02
CUI: C2673954
Disease: Absent skin pigmentation
Absent skin pigmentation 		1 0 1 0.50 0 0
CUI: C2677190
Disease: SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 3 (disorder)
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 3 (disorder) 		1 13 1 0.50 13 0.93
CUI: C3149136
Disease: SKIN/HAIR/EYE PIGMENTATION 3, BLUE/GREEN EYES
SKIN/HAIR/EYE PIGMENTATION 3, BLUE/GREEN EYES 		1 1 1 0.50 1 7.1E-02
CUI: C3806221
Disease: Giant melanosomes in melanocytes
Giant melanosomes in melanocytes 		4 0 2 0.50 0 0
CUI: C4310625
Disease: COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS 		1 0 1 0.50 0 0
CUI: C4750999
Disease: Ocular albinism with congenital sensorineural deafness
Ocular albinism with congenital sensorineural deafness 		1 0 1 0.50 0 0
CUI: C0022078
Disease: Iris Diseases
Iris Diseases 		2 0 1 0.33 0 0
CUI: C0221436
Disease: Melanoderma (disorder)
Melanoderma (disorder) 		2 0 1 0.33 0 0
CUI: C0268503
Disease: Autosomal recessive ocular albinism
Autosomal recessive ocular albinism 		2 4 1 0.33 1 5.9E-02
CUI: C0339619
Disease: Congenital esotropia
Congenital esotropia 		2 0 1 0.33 0 0
CUI: C0342552
Disease: Autoimmune endocrine disease
Autoimmune endocrine disease 		2 0 1 0.33 0 0
CUI: C1332614
Disease: Angiosarcoma of the breast
Angiosarcoma of the breast 		2 0 1 0.33 0 0