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
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
C0432072 Dysmorphic features disease Congenital Abnormality 335
C0428474 Serum LDL cholesterol measurement phenotype Laboratory Procedure 269
C1861324 Short philtrum phenotype Finding Abnormality of head or neck 182
C3828530 Platelet Component Distribution Width Measurement phenotype Laboratory Procedure 134
C0426429 Broad nasal tip phenotype Finding Abnormality of head or neck 125
C1839758 Narrow forehead phenotype Finding Abnormality of head or neck 106
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
C0857379 Abnormality of the pinna phenotype Finding Abnormality of the ear 85
C1842366 Low anterior hairline phenotype Finding Abnormality of the integument; Abnormality of head or neck 71
C1858036 Periorbital fullness phenotype Finding Abnormality of head or neck 57
C1848529 Hypoplasia of the pons phenotype Finding Abnormality of the nervous system 30
C0523744 Lipids measurement group Laboratory Procedure 27
C4014492 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23 disease Disease or Syndrome disease of anatomical entity 1
C0001948 Alcohol consumption phenotype Behavior and Behavior Mechanisms Individual Behavior 210
C0007222 Cardiovascular Diseases group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 235
C0423113 Telecanthus phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Finding Abnormality of head or neck 134
C1857970 Hypobetalipoproteinemia, Familial, 2 disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome genetic disease; disease of metabolism 2