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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 2.2E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.3E-03
CUI: C0162539
Disease: IgG Deficiency disorder
IgG Deficiency disorder 		0 2 0 0 1 2.3E-03
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma 		0 1 0 0 1 2.3E-03
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 6 0 0 1 2.2E-03
CUI: C0278139
Disease: Moderate pain
Moderate pain 		0 1 0 0 1 2.3E-03
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		0 4 0 0 1 2.3E-03
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		0 21 0 0 1 2.2E-03
CUI: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		0 19 0 0 1 2.2E-03
CUI: C0476482
Disease: Restlessness and agitation
Restlessness and agitation 		0 1 0 0 1 2.3E-03
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		0 21 0 0 1 2.2E-03
CUI: C0860602
Disease: Anxious personality
Anxious personality 		0 2 0 0 1 2.3E-03
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		0 3 0 0 1 2.3E-03
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		0 3 0 0 1 2.3E-03
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		0 9 0 0 2 4.5E-03
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
ALZHEIMER DISEASE, SUSCEPTIBILITY TO 		0 3 0 0 1 2.3E-03
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder) 		0 1 0 0 1 2.3E-03
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE 		0 26 0 0 1 2.1E-03
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		0 1 0 0 1 2.3E-03
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		0 1 0 0 1 2.3E-03
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		0 2 0 0 1 2.3E-03
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		0 1 0 0 1 2.3E-03
CUI: C3178803
Disease: Social Anhedonia
Social Anhedonia 		0 4 0 0 1 2.3E-03
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		0 2 0 0 1 2.3E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.3E-03