Source: GWASCAT

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0023980 Longevity phenotype Temporal Concept 48 74
C0018681 Headache phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom Abnormality of the nervous system 18 28
C0574785 Lower Urinary Tract Symptoms phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 13 23
C0027769 Nervousness phenotype Behavior and Behavior Mechanisms Sign or Symptom 6 12
C0004604 Back Pain phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom Constitutional symptom; Abnormality of the skeletal system 3 4
C0011991 Diarrhea phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom disease of anatomical entity Abnormality of the digestive system 3 3
C3899405 Decreased Attention phenotype Sign or Symptom 2 2
C0030193 Pain phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom Constitutional symptom 1 5
C0037383 Sneezing phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom Abnormality of the respiratory system 1 2
C0231749 Knee pain phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Sign or Symptom Constitutional symptom 1 4
C0751093 Dystonia, Limb phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom Abnormality of the nervous system 1 1
C4042861 Obesity, Metabolically Benign phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Sign or Symptom 1 6
C0020450 Hyperemesis Gravidarum phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Sign or Symptom Abnormality of prenatal development or birth 0 2
C2242456 thyroid function phenotype Physiologic Function 4 5
C0005848 Blood Viscosity phenotype Physiologic Function 1 1
C1527304 Allergic Reaction phenotype Immune System Diseases Pathologic Function disease of anatomical entity 104 234
C1611184 Calcification of coronary artery phenotype Nutritional and Metabolic Diseases; Cardiovascular Diseases Pathologic Function Abnormality of the skeletal system; Abnormality of the cardiovascular system 45 84
C0085298 Sudden Cardiac Death phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function Abnormality of the cardiovascular system 20 32
C0015944 Fetal Membranes, Premature Rupture phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function Abnormality of prenatal development or birth 14 21
C4268744 Atypical femoral fracture phenotype Pathologic Function 12 23
C0034065 Pulmonary Embolism disease Respiratory Tract Diseases; Cardiovascular Diseases Pathologic Function disease of anatomical entity Abnormality of the respiratory system; Abnormality of the cardiovascular system 9 12
C0151526 Premature Birth phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function Abnormality of prenatal development or birth 7 10
C0948364 Periprosthetic osteolysis phenotype Musculoskeletal Diseases Pathologic Function 5 6
C0021655 Insulin Resistance phenotype Nutritional and Metabolic Diseases Pathologic Function Abnormality of metabolism/homeostasis 4 10
C0029445 Bone necrosis phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Pathologic Function disease of anatomical entity Abnormality of the skeletal system 4 5