Source: CTD_human

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0334583 Pilocytic Astrocytoma disease Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation 25
C0031099 Periodontitis disease Stomatognathic Diseases Disease or Syndrome disease of anatomical entity Abnormality of the immune system; Abnormality of head or neck 3
C0031051 Pericementitis disease Stomatognathic Diseases Disease or Syndrome 3
C0030297 Pancreatic Neoplasm disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation Abnormality of the digestive system; Neoplasm 94
C0264393 Panacinar Emphysema disease Respiratory Tract Diseases Disease or Syndrome 12
C0029172 Oral Submucous Fibrosis disease Stomatognathic Diseases Disease or Syndrome disease of anatomical entity 18
C0028754 Obesity disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome disease of metabolism Growth abnormality 186
C0007131 Non-Small Cell Lung Carcinoma disease Neoplasms; Respiratory Tract Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation Neoplasm; Abnormality of the respiratory system 139
C0007621 Neoplastic Cell Transformation phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 139
C0027627 Neoplasm Metastasis phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 217
C0027626 Neoplasm Invasiveness phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Pathologic Function 184
C2936381 Neointima Formation phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 6
C2936380 Neointima disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 6
C0027051 Myocardial Infarction disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 95
C0026766 Multiple Organ Failure phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 8
C0026552 Morphine Dependence disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction disease of mental health 7
C0600272 Morphine Abuse disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 7
C0547065 Mixed oligoastrocytoma disease Neoplasms Neoplastic Process disease of cellular proliferation 25
C0740376 Middle Cerebral Artery Thrombosis disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34
C0238281 Middle Cerebral Artery Syndrome phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34
C0740391 Middle Cerebral Artery Occlusion disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 34
C0751845 Middle Cerebral Artery Embolus phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 34
C0521174 Microcalcification phenotype Nutritional and Metabolic Diseases Pathologic Function 42
C2751322 Metaphyseal Anadysplasia 2 disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 1
C4721845 Marfan Syndrome, Type I disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 9