Source: INFERRED ×
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: C1840598
Disease: FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 2
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 2 		0 1 0 0 1 6.3E-04
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 		0 34 0 0 1 6.1E-04
CUI: C4050627
Disease: Soluble P-Selectin Measurement
Soluble P-Selectin Measurement 		0 3 0 0 1 6.2E-04
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease 		0 43 0 0 1 6.1E-04
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		1 0 1 1.4E-03 0 0
CUI: C0002875
Disease: Cooley's anemia
Cooley's anemia 		1 0 1 1.4E-03 0 0
CUI: C0005283
Disease: beta Thalassemia
beta Thalassemia 		1 85 1 1.4E-03 1 5.9E-04
CUI: C0005818
Disease: Blood Platelet Disorders
Blood Platelet Disorders 		1 0 1 1.4E-03 0 0
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		1 0 1 1.4E-03 0 0
CUI: C0014522
Disease: Epidermodysplasia Verruciformis
Epidermodysplasia Verruciformis 		1 0 1 1.4E-03 0 0
CUI: C0017926
Disease: Glycogen Storage Disease Type VII
Glycogen Storage Disease Type VII 		1 0 1 1.4E-03 0 0
CUI: C0018799
Disease: Heart Diseases
Heart Diseases 		1 0 1 1.4E-03 0 0
CUI: C0019045
Disease: Hemoglobinopathies
Hemoglobinopathies 		1 0 1 1.4E-03 0 0
CUI: C0019937
Disease: Horner Syndrome
Horner Syndrome 		1 0 1 1.4E-03 0 0
CUI: C0020075
Disease: Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory Autonomic Neuropathy, Type 5 		1 0 1 1.4E-03 0 0
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III 		1 0 1 1.4E-03 0 0
CUI: C0022350
Disease: Jaundice, Chronic Idiopathic
Jaundice, Chronic Idiopathic 		1 0 1 1.4E-03 0 0
CUI: C0023003
Disease: Langer-Giedion Syndrome
Langer-Giedion Syndrome 		1 0 1 1.4E-03 0 0
CUI: C0024748
Disease: alpha-Mannosidosis
alpha-Mannosidosis 		1 0 1 1.4E-03 0 0
CUI: C0028756
Disease: Obesity, Morbid
Obesity, Morbid 		1 0 1 1.4E-03 0 0
CUI: C0032197
Disease: Platelet Storage Pool Deficiency
Platelet Storage Pool Deficiency 		1 0 1 1.4E-03 0 0
CUI: C0033117
Disease: Priapism
Priapism 		1 0 1 1.4E-03 0 0
CUI: C0034902
Disease: Pure Red-Cell Aplasia
Pure Red-Cell Aplasia 		1 0 1 1.4E-03 0 0
CUI: C0086664
Disease: Myelocele
Myelocele 		1 0 1 1.4E-03 0 0
CUI: C0152169
Disease: Renal Colic
Renal Colic 		1 0 1 1.4E-03 0 0