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: C0018862
Disease: Heberden node
Heberden node 		0 1 0 0 1 1.3E-02
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		0 1 0 0 1 1.3E-02
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		0 6 0 0 1 1.2E-02
CUI: C0272024
Disease: Secondary acquired sideroblastic anemia
Secondary acquired sideroblastic anemia 		0 2 0 0 1 1.2E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 2.5E-02
CUI: C0342800
Disease: Inosine Triphosphatase Deficiency
Inosine Triphosphatase Deficiency 		0 4 0 0 1 1.2E-02
CUI: C0373607
Disease: Ferritin measurement
Ferritin measurement 		0 21 0 0 1 1.0E-02
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		0 21 0 0 1 1.0E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 1 1.2E-02
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		0 3 0 0 1 1.2E-02
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0 81 0 0 1 6.3E-03
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0 95 0 0 1 5.7E-03
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE 		0 26 0 0 1 9.5E-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 1.2E-02
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		0 2 0 0 1 1.2E-02
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		134 0 1 1.6E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color 		130 0 1 1.6E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause 		129 0 1 1.6E-03 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities 		112 0 1 1.6E-03 0 0
CUI: C1853487
Disease: Thick eyebrow
Thick eyebrow 		104 0 1 1.7E-03 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		104 0 1 1.7E-03 0 0
CUI: C0234376
Disease: Action Tremor
Action Tremor 		95 0 1 1.7E-03 0 0
CUI: C1846460
Disease: Abnormality of the outer ear
Abnormality of the outer ear 		95 0 1 1.7E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 1 1.7E-03 0 0
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		90 0 1 1.7E-03 0 0