Source: RGD

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0007787 Transient Ischemic Attack disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 170
C0027055 Myocardial Reperfusion Injury phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 161
C0740392 Infarction, Middle Cerebral Artery disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome disease of anatomical entity 108
C0752308 Hypoxia-Ischemia, Brain disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 67
C0872084 Sarcopenia phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 14
C0220701 RETINITIS PIGMENTOSA 1 disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome genetic disease; disease of anatomical entity 8
C1262037 Diabetic cystopathy disease Disease or Syndrome 3
C0035305 Retinal Detachment disease Eye Diseases Disease or Syndrome disease of anatomical entity Abnormality of the eye 11
C0035334 Retinitis Pigmentosa disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome disease of anatomical entity Abnormality of the eye 8