Source: CURATED

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0004238 Atrial Fibrillation disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 160 374
C2985280 Blood Protein Measurement phenotype Laboratory Procedure 0 2575
C1305855 Body mass index phenotype Clinical Attribute 0 2689
C1611184 Calcification of coronary artery phenotype Nutritional and Metabolic Diseases; Cardiovascular Diseases Pathologic Function Abnormality of the skeletal system; Abnormality of the cardiovascular system 0 205
C0007222 Cardiovascular Diseases group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 36 342
C0038454 Cerebrovascular accident group Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the nervous system; Abnormality of the cardiovascular system 62 198
C1956346 Coronary Artery Disease disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 65 627
C0010068 Coronary heart disease disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 24 469
C4528257 Corpuscular Hemoglobin Concentration Mean phenotype Laboratory or Test Result 0 4389
C0011847 Diabetes disease Endocrine System Diseases Disease or Syndrome disease of metabolism 3 104
C0011849 Diabetes Mellitus group Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome disease of metabolism Abnormality of metabolism/homeostasis; Abnormality of the endocrine system 32 118
C0428883 Diastolic blood pressure phenotype Clinical Attribute 0 1037
C0495706 elevated blood glucose level phenotype Finding 0 111
C0200638 Eosinophil count procedure phenotype Laboratory Procedure 0 1144
C0337438 Glucose measurement phenotype Laboratory Procedure 0 111
C0018801 Heart failure disease Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 110 82
C0018935 Hematocrit procedure phenotype Laboratory Procedure 0 216
C0392885 High density lipoprotein measurement phenotype Laboratory Procedure 0 1440
C0020557 Hypertriglyceridemia phenotype Nutritional and Metabolic Diseases Disease or Syndrome 15 18
C0202117 Low density lipoprotein cholesterol measurement phenotype Laboratory Procedure 0 1142
C0006826 Malignant Neoplasms group Neoplasms Neoplastic Process disease of cellular proliferation Neoplasm 128 202
C0524620 Metabolic Syndrome X disease Nutritional and Metabolic Diseases Disease or Syndrome genetic disease; syndrome 21 124
C0202177 Phospholipid measurement phenotype Laboratory Procedure 0 306
C3828530 Platelet Component Distribution Width Measurement phenotype Laboratory Procedure 0 200
C0200665 Platelet mean volume determination (procedure) phenotype Laboratory Procedure 0 371