Anemia due to intrinsic red cell abnormality   323666000

SNOMED CT code


SNOMED code323666000
nameAnemia due to intrinsic red cell abnormality
statusactive
date introduced2002-01-31
fully specified name(s)Anemia due to intrinsic red cell abnormality (disorder)
synonyms
  • Anaemia due to intrinsic red cell abnormality
  • Anemia due to intrinsic red cell abnormality
parentsAnemia   271737000
children
  • Anemia due to membrane defect   111575000
  • Hb S disease   127040003
  • Hereditary elliptocytosis due to abnormal protein 4.1   75443009
  • Hereditary elliptocytosis due to alpha spectrin defect   8857001
  • Hereditary elliptocytosis due to beta spectrin defect in self-association   73073009
  • Hereditary elliptocytosis due to beta spectrin-ankyrin interaction   66262001
  • Hereditary elliptocytosis due to deficiency of protein 4.1   5994005
  • Hereditary elliptocytosis due to glycophorin C deficiency   15121005
  • Hereditary pyropoikilocytosis   9434008
  • Paroxysmal nocturnal hemoglobinuria   1963002
  • Rh deficiency syndrome   37272000
  • Stomatocytosis   3272007
  • Xerocytosis   87994004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of blood, lymphatics and immune system   299691001
      Disorder of cellular component of blood   414022008
        Anemia   271737000
          Anemia due to intrinsic red cell abnormality   323666000

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