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: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 6 2 0.50 2 0.29
CUI: C3805877
Disease: Hyperpigmentation in sun-exposed areas
Hyperpigmentation in sun-exposed areas 		3 0 2 0.40 0 0
CUI: C1263733
Disease: Uroporphyrinuria
Uroporphyrinuria 		4 0 2 0.33 0 0
CUI: C0003756
Disease: Arenaviridae Infections
Arenaviridae Infections 		1 0 1 0.25 0 0
CUI: C0153500
Disease: Malignant neoplasm of heart
Malignant neoplasm of heart 		1 0 1 0.25 0 0
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 1 1 0.25 1 0.33
CUI: C0342861
Disease: Uroporphyrinogen decarboxylase deficiency
Uroporphyrinogen decarboxylase deficiency 		1 0 1 0.25 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 0.25 0 0
CUI: C1867968
Disease: Porphyria Cutanea Tarda, Type I
Porphyria Cutanea Tarda, Type I 		1 0 1 0.25 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 1 1 0.25 1 0.33
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 1 1 0.25 1 0.33
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 2 1 0.25 2 0.67
CUI: C2931631
Disease: Chromosome 7, trisomy mosaic
Chromosome 7, trisomy mosaic 		1 0 1 0.25 0 0
CUI: C2931707
Disease: Chromosome 15, trisomy mosaicism
Chromosome 15, trisomy mosaicism 		1 0 1 0.25 0 0
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 1 1 0.25 1 0.33
CUI: C3266753
Disease: Severe left ventricular systolic dysfunction
Severe left ventricular systolic dysfunction 		1 0 1 0.25 0 0
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		1 2 1 0.25 2 0.67
CUI: C3711388
Disease: African Hemochromatosis
African Hemochromatosis 		1 0 1 0.25 0 0
CUI: C4225219
Disease: IMMUNODEFICIENCY 46
IMMUNODEFICIENCY 46 		1 0 1 0.25 0 0
CUI: C4275028
Disease: Paternal uniparental disomy of chromosome 20
Paternal uniparental disomy of chromosome 20 		1 0 1 0.25 0 0
CUI: C4546184
Disease: Imprinting error
Imprinting error 		1 0 1 0.25 0 0
CUI: C4707010
Disease: Mosaic trisomy 2 syndrome
Mosaic trisomy 2 syndrome 		1 0 1 0.25 0 0
CUI: C0151861
Disease: Porphyruria
Porphyruria 		2 0 1 0.20 0 0
CUI: C0342886
Disease: Primary hypertriglyceridemia
Primary hypertriglyceridemia 		2 0 1 0.20 0 0
CUI: C0948120
Disease: Hepatic siderosis
Hepatic siderosis 		8 0 2 0.20 0 0