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: C1847132
Disease: ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE
ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE 		1 0 1 8.3E-02 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 0 1 8.3E-02 0 0
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 0 1 8.3E-02 0 0
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 2 1 8.3E-02 1 5.9E-02
CUI: C2673954
Disease: Absent skin pigmentation
Absent skin pigmentation 		1 0 1 8.3E-02 0 0
CUI: C2677190
Disease: SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 3 (disorder)
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 3 (disorder) 		1 0 1 8.3E-02 0 0
CUI: C3149136
Disease: SKIN/HAIR/EYE PIGMENTATION 3, BLUE/GREEN EYES
SKIN/HAIR/EYE PIGMENTATION 3, BLUE/GREEN EYES 		1 0 1 8.3E-02 0 0
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 0 1 8.3E-02 0 0
CUI: C3266753
Disease: Severe left ventricular systolic dysfunction
Severe left ventricular systolic dysfunction 		1 0 1 8.3E-02 0 0
CUI: C3277918
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1 		1 0 1 8.3E-02 0 0
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		1 2 1 8.3E-02 1 5.9E-02
CUI: C3889615
Disease: TRANSFERRIN VARIANT D1 PHENOTYPE
TRANSFERRIN VARIANT D1 PHENOTYPE 		1 0 1 8.3E-02 0 0
CUI: C3889617
Disease: TRANSFERRIN VARIANT B2 PHENOTYPE
TRANSFERRIN VARIANT B2 PHENOTYPE 		1 0 1 8.3E-02 0 0
CUI: C3889619
Disease: TRANSFERRIN VARIANT Bv PHENOTYPE
TRANSFERRIN VARIANT Bv PHENOTYPE 		1 0 1 8.3E-02 0 0
CUI: C4225610
Disease: TRANSFERRIN VARIANT D(CHI)
TRANSFERRIN VARIANT D(CHI) 		1 0 1 8.3E-02 0 0
CUI: C4703592
Disease: Elevated hepcidin level
Elevated hepcidin level 		1 0 1 8.3E-02 0 0
CUI: C0022078
Disease: Iris Diseases
Iris Diseases 		2 0 1 7.7E-02 0 0
CUI: C0078921
Disease: Albinism, Tyrosinase-Negative
Albinism, Tyrosinase-Negative 		2 0 1 7.7E-02 0 0
CUI: C0078922
Disease: Albinism, Tyrosinase-Positive
Albinism, Tyrosinase-Positive 		2 0 1 7.7E-02 0 0
CUI: C0078923
Disease: Albinism, Yellow-Mutant
Albinism, Yellow-Mutant 		2 0 1 7.7E-02 0 0
CUI: C0151861
Disease: Porphyruria
Porphyruria 		2 0 1 7.7E-02 0 0
CUI: C0221436
Disease: Melanoderma (disorder)
Melanoderma (disorder) 		2 0 1 7.7E-02 0 0
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 6 1 7.7E-02 1 4.8E-02
CUI: C0268503
Disease: Autosomal recessive ocular albinism
Autosomal recessive ocular albinism 		2 0 1 7.7E-02 0 0
CUI: C0339619
Disease: Congenital esotropia
Congenital esotropia 		2 0 1 7.7E-02 0 0