Source: CTD_mouse

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0013595 Eczema disease Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity Abnormality of the integument; Abnormality of the immune system 1
C0037274 Dermatologic disorders group Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity Abnormality of the integument 1
C0024115 Lung diseases group Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity Abnormality of the respiratory system 2
C0085129 Bronchial Hyperreactivity disease Respiratory Tract Diseases Disease or Syndrome 1
C1800706 Idiopathic Pulmonary Fibrosis disease Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity 1
C4721508 Hamman-Rich Disease disease Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity 1
C4721509 Usual Interstitial Pneumonia disease Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity Abnormality of the respiratory system 1
C4721952 Familial Idiopathic Pulmonary Fibrosis disease Respiratory Tract Diseases Disease or Syndrome disease of anatomical entity 1
C0022283 Incontinentia Pigmenti Achromians disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Congenital Abnormality disease of anatomical entity 1
C0036305 Schamberg Disease phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 1
C0549567 Pigmentation Disorders group Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity 1
C0028754 Obesity disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome disease of metabolism Growth abnormality 3
C0238281 Middle Cerebral Artery Syndrome phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1
C0740376 Middle Cerebral Artery Thrombosis disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1
C0740391 Middle Cerebral Artery Occlusion disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 1
C0740392 Infarction, Middle Cerebral Artery disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 1
C0751845 Middle Cerebral Artery Embolus phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1
C0751846 Left Middle Cerebral Artery Infarction phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1
C0751847 Embolic Infarction, Middle Cerebral Artery phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1
C0751848 Thrombotic Infarction, Middle Cerebral Artery phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1
C0751849 Right Middle Cerebral Artery Infarction phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1
C0022333 Jacksonian Seizure disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome disease of anatomical entity 1
C0027854 Neurologic Manifestations phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 1
C0036572 Seizures phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom disease of anatomical entity Abnormality of the nervous system 1
C0038220 Status Epilepticus disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the nervous system 1