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: C0523522
Disease: beta-Endorphin measurement
beta-Endorphin measurement 		2 0 2 0.29 0 0
CUI: C2675207
Disease: URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4
URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4 		1 0 1 0.14 0 0
CUI: C4703592
Disease: Elevated hepcidin level
Elevated hepcidin level 		1 0 1 0.14 0 0
CUI: C4748455
Disease: SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE
SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE 		1 0 1 0.14 0 0
CUI: C0740989
Disease: Chronic iron deficiency anaemia
Chronic iron deficiency anaemia 		2 0 1 0.12 0 0
CUI: C4015831
Disease: APOLIPOPROTEIN A-I (MARBURG) PHENOTYPE
APOLIPOPROTEIN A-I (MARBURG) PHENOTYPE 		2 0 1 0.12 0 0
CUI: C4015834
Disease: APOLIPOPROTEIN A-I (MUNSTER3C) PHENOTYPE
APOLIPOPROTEIN A-I (MUNSTER3C) PHENOTYPE 		2 0 1 0.12 0 0
CUI: C4015835
Disease: APOLIPOPROTEIN A-I (MUNSTER3B) PHENOTYPE
APOLIPOPROTEIN A-I (MUNSTER3B) PHENOTYPE 		2 0 1 0.12 0 0
CUI: C4015839
Disease: APOLIPOPROTEIN A-I (BALTIMORE) PHENOTYPE
APOLIPOPROTEIN A-I (BALTIMORE) PHENOTYPE 		2 0 1 0.12 0 0
CUI: C4015843
Disease: AMYLOIDOSIS, CARDIAC AND CUTANEOUS
AMYLOIDOSIS, CARDIAC AND CUTANEOUS 		2 0 1 0.12 0 0
CUI: C4017713
Disease: APOLIPOPROTEIN A-I (NORWAY) PHENOTYPE
APOLIPOPROTEIN A-I (NORWAY) PHENOTYPE 		2 0 1 0.12 0 0
CUI: C4551500
Disease: Amyloid Polyneuropathy, Iowa Type
Amyloid Polyneuropathy, Iowa Type 		3 0 1 0.11 0 0
CUI: C0031873
Disease: Pica Disease
Pica Disease 		5 3 1 9.1E-02 1 0.11
CUI: C0342749
Disease: GLYCOGEN STORAGE DISEASE Ic
GLYCOGEN STORAGE DISEASE Ic 		5 0 1 9.1E-02 0 0
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement 		6 10 1 8.3E-02 1 6.2E-02
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		6 10 1 8.3E-02 1 6.2E-02
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE 		7 26 1 7.7E-02 1 3.1E-02
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		8 0 1 7.1E-02 0 0
CUI: C1851714
Disease: Sclerosis of skull base
Sclerosis of skull base 		8 0 1 7.1E-02 0 0
CUI: C0342471
Disease: 3 beta-Hydroxysteroid dehydrogenase deficiency
3 beta-Hydroxysteroid dehydrogenase deficiency 		9 0 1 6.7E-02 0 0
CUI: C0700639
Disease: Pyloric Stenosis, Hypertrophic
Pyloric Stenosis, Hypertrophic 		26 0 2 6.5E-02 0 0
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		10 21 1 6.2E-02 1 3.7E-02
CUI: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		10 19 1 6.2E-02 1 4.0E-02
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		10 21 1 6.2E-02 1 3.7E-02
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		10 0 1 6.2E-02 0 0