Source: INFERRED

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0557874 Global developmental delay disease Mental or Behavioral Dysfunction Abnormality of the nervous system 1458
C0036572 Seizures phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom disease of anatomical entity Abnormality of the nervous system 1292
C2985280 Blood Protein Measurement phenotype Laboratory Procedure 1156
C0202236 Triglycerides measurement phenotype Laboratory Procedure 563
C0392885 High density lipoprotein measurement phenotype Laboratory Procedure 545
C1445957 Serum total cholesterol measurement phenotype Laboratory Procedure 486
C0202117 Low density lipoprotein cholesterol measurement phenotype Laboratory Procedure 483
C0523465 Serum albumin measurement phenotype Laboratory Procedure 433
C0344482 Hypoplasia of corpus callosum disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality Abnormality of the nervous system 351
C0432072 Dysmorphic features disease Congenital Abnormality 335
C0428474 Serum LDL cholesterol measurement phenotype Laboratory Procedure 269
C0010346 Crohn Disease disease Digestive System Diseases Disease or Syndrome genetic disease; disease of anatomical entity Abnormality of the digestive system; Abnormality of the immune system 266
C0007222 Cardiovascular Diseases group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 235
C0001948 Alcohol consumption phenotype Behavior and Behavior Mechanisms Individual Behavior 210
C1861324 Short philtrum phenotype Finding Abnormality of head or neck 182
C0684276 Hypsarrhythmia phenotype Nervous System Diseases Finding Abnormality of the nervous system 146
C3828530 Platelet Component Distribution Width Measurement phenotype Laboratory Procedure 134
C0423113 Telecanthus phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Finding Abnormality of head or neck 134
C4048268 Cortical visual impairment phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Pathologic Function Abnormality of the eye 133
C0426429 Broad nasal tip phenotype Finding Abnormality of head or neck 125
C3810365 Central visual impairment disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome Abnormality of the eye 115
C1839758 Narrow forehead phenotype Finding Abnormality of head or neck 106
C0543888 Epileptic encephalopathy disease Nervous System Diseases Disease or Syndrome Abnormality of the nervous system 105
C1853487 Thick eyebrow phenotype Finding Abnormality of the integument; Abnormality of head or neck 104
C1836543 Thick vermilion border phenotype Finding Abnormality of head or neck 95