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: C3539168
Disease: PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A
PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A 		0 3 0 0 1 1.4E-02
CUI: C0031911
Disease: Pigmentation
Pigmentation 		1 0 1 4.2E-02 0 0
CUI: C0268499
Disease: Autosomal dominant oculocutaneous albinism
Autosomal dominant oculocutaneous albinism 		1 0 1 4.2E-02 0 0
CUI: C0268500
Disease: Yellow mutant oculocutaneous albinism
Yellow mutant oculocutaneous albinism 		1 0 1 4.2E-02 0 0
CUI: C0333008
Disease: Congenital hypopigmentation
Congenital hypopigmentation 		1 0 1 4.2E-02 0 0
CUI: C0346977
Disease: Secondary malignant neoplasm of spleen
Secondary malignant neoplasm of spleen 		1 0 1 4.2E-02 0 0
CUI: C1313983
Disease: Acute contagious conjunctivitis
Acute contagious conjunctivitis 		1 0 1 4.2E-02 0 0
CUI: C1847024
Disease: ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder)
ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder) 		1 24 1 4.2E-02 1 1.1E-02
CUI: C1847132
Disease: ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE
ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE 		1 2 1 4.2E-02 1 1.4E-02
CUI: C1847836
Disease: Oculocutaneous Albinism, Type IV
Oculocutaneous Albinism, Type IV 		1 0 1 4.2E-02 0 0
CUI: C1856796
Disease: Estren-Dameshek Variant of Fanconi Anemia
Estren-Dameshek Variant of Fanconi Anemia 		1 0 1 4.2E-02 0 0
CUI: C1856797
Disease: Estren-Dameshek Variant of Fanconi Pancytopenia
Estren-Dameshek Variant of Fanconi Pancytopenia 		1 0 1 4.2E-02 0 0
CUI: C2673265
Disease: Skin-Hair-Eye Pigmentation, Variation In, 8
Skin-Hair-Eye Pigmentation, Variation In, 8 		1 1 1 4.2E-02 1 1.4E-02
CUI: C2673584
Disease: SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 5 (disorder)
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 5 (disorder) 		1 0 1 4.2E-02 0 0
CUI: C2673954
Disease: Absent skin pigmentation
Absent skin pigmentation 		1 0 1 4.2E-02 0 0
CUI: C2676042
Disease: Skin-Hair-Eye Pigmentation, Variation In, 4
Skin-Hair-Eye Pigmentation, Variation In, 4 		1 0 1 4.2E-02 0 0
CUI: C2677190
Disease: SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 3 (disorder)
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 3 (disorder) 		1 13 1 4.2E-02 1 1.2E-02
CUI: C2678403
Disease: UV-INDUCED SKIN DAMAGE, SUSCEPTIBILITY TO
UV-INDUCED SKIN DAMAGE, SUSCEPTIBILITY TO 		1 0 1 4.2E-02 0 0
CUI: C2698751
Disease: Pediatric nodal marginal zone lymphoma
Pediatric nodal marginal zone lymphoma 		1 0 1 4.2E-02 0 0
CUI: C2751295
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5 		1 0 1 4.2E-02 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 4.2E-02 2 2.8E-02
CUI: C3149136
Disease: SKIN/HAIR/EYE PIGMENTATION 3, BLUE/GREEN EYES
SKIN/HAIR/EYE PIGMENTATION 3, BLUE/GREEN EYES 		1 1 1 4.2E-02 1 1.4E-02
CUI: C3151465
Disease: PROTEIN Z DEFICIENCY
PROTEIN Z DEFICIENCY 		1 0 1 4.2E-02 0 0
CUI: C3553886
Disease: MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE 		1 0 1 4.2E-02 0 0
CUI: C3647231
Disease: Oculocutaneous albinism type 4
Oculocutaneous albinism type 4 		1 0 1 4.2E-02 0 0