Source: GWASCAT

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0042834 Vital capacity phenotype Clinical Attribute 430 746
C0017654 Glomerular Filtration Rate phenotype Diagnostic Procedure 399 1031
C0201976 Creatinine measurement, serum (procedure) phenotype Laboratory Procedure 124 243
C0523953 Cardiac troponin T measurement phenotype Laboratory Procedure 11 16
C0020608 Hypodontia disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Congenital Abnormality disease of anatomical entity Abnormality of head or neck 5 8
C0155922 Tooth development and eruption disorder disease Mental Disorders; Stomatognathic Diseases Disease or Syndrome 5 8
C0399352 Developmental absence of tooth disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Congenital Abnormality disease of anatomical entity Abnormality of head or neck 5 8
C1970117 Tooth Agenesis, Selective, With Orofacial Cleft disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases Disease or Syndrome disease of anatomical entity 5 8
C1970118 Hypodontia Oligodontia with Orofacial Cleft disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases Disease or Syndrome disease of anatomical entity 5 8
C3489529 Tooth Agenesis, Familial disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Congenital Abnormality disease of anatomical entity 5 8
C4082304 Oligodontia disease Congenital Abnormality disease of anatomical entity Abnormality of head or neck 5 8
C4310638 TOOTH AGENESIS, SELECTIVE, 9 disease Congenital Abnormality 5 8