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: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		10 19 3 0.21 4 9.8E-02
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement 		6 10 2 0.18 2 5.9E-02
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		6 10 2 0.18 2 5.9E-02
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 1 1 0.14 1 3.8E-02
CUI: C0472792
Disease: Hemolytic anemia due to hexokinase deficiency
Hemolytic anemia due to hexokinase deficiency 		1 0 1 0.14 0 0
CUI: C0796055
Disease: Mercaptolactate-Cysteine Disulfiduria
Mercaptolactate-Cysteine Disulfiduria 		1 0 1 0.14 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 0.14 0 0
CUI: C1531500
Disease: Alpha carotene level
Alpha carotene level 		1 0 1 0.14 0 0
CUI: C1833236
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder)
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder) 		1 0 1 0.14 0 0
CUI: C1849813
Disease: Glycogen Storage Disease of Heart, Lethal Congenital
Glycogen Storage Disease of Heart, Lethal Congenital 		1 0 1 0.14 0 0
CUI: C1854449
Disease: Neuropathy, hereditary motor and sensory, Russe type
Neuropathy, hereditary motor and sensory, Russe type 		1 0 1 0.14 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 1 1 0.14 1 3.8E-02
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 1 1 0.14 1 3.8E-02
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 2 1 0.14 2 7.7E-02
CUI: C2936458
Disease: Fasciculoventricular Accessory Pathway
Fasciculoventricular Accessory Pathway 		1 0 1 0.14 0 0
CUI: C2936459
Disease: Nodoventricular Accessory Pathway
Nodoventricular Accessory Pathway 		1 0 1 0.14 0 0
CUI: C3150343
Disease: HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY
HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY 		1 0 1 0.14 0 0
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 1 1 0.14 1 3.8E-02
CUI: C3266753
Disease: Severe left ventricular systolic dysfunction
Severe left ventricular systolic dysfunction 		1 0 1 0.14 0 0
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		1 2 1 0.14 2 7.7E-02
CUI: C4016809
Disease: WOLFF-PARKINSON-WHITE SYNDROME, CHILDHOOD-ONSET
WOLFF-PARKINSON-WHITE SYNDROME, CHILDHOOD-ONSET 		1 0 1 0.14 0 0
CUI: C4025004
Disease: Ventricular preexcitation with multiple accessory pathways
Ventricular preexcitation with multiple accessory pathways 		1 0 1 0.14 0 0
CUI: C4479526
Disease: RETINITIS PIGMENTOSA 79
RETINITIS PIGMENTOSA 79 		1 0 1 0.14 0 0
CUI: C4703592
Disease: Elevated hepcidin level
Elevated hepcidin level 		1 0 1 0.14 0 0
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		10 21 2 0.13 3 6.8E-02