Erythrocyte enzyme deficiency   234401000

SNOMED CT code


SNOMED code234401000
nameErythrocyte enzyme deficiency
statusactive
date introduced2002-01-31
fully specified name(s)Erythrocyte enzyme deficiency (disorder)
synonymsErythrocyte enzyme deficiency
attributes - group1
Finding siteErythrocyte   41898006
parentsRed blood cell disorder   38292009
children
  • Adenosine deaminase overproduction   234408006
  • Chronic non-spherocytic hemolytic anemia   234402007
  • Deficiency of glucose-6-phosphate dehydrogenase   124134002
  • Deficiency of glutathione reductase (NAD(P)H)   124188007
  • Deficiency of hexokinase   124297004
  • Dehydrated hereditary stomatocytosis   715526002
  • Familial pseudohyperkalemia   717254007
  • Glucose phosphate isomerase deficiency   234404008
  • Hereditary stomatocytosis   14087004
  • HNSHA due to decreased adenosine deaminase activity   78908001
  • HNSHA due to diphosphoglycerate mutase deficiency   62268000
  • HNSHA due to gamma glutamyl cysteine synthetase deficiency   25251008
  • HNSHA due to glutathione synthetase deficiency   111579006
  • HNSHA due to hexokinase deficiency   42484009
  • HNSHA due to NADH diaphorase deficiency   47526003
  • HNSHA due to phosphofructokinase deficiency   41387000
  • HNSHA due to phosphoglycerate kinase deficiency   59644002
  • HNSHA due to pyrimidine-5'-nucleotidase deficiency   34194007
  • HNSHA due to triosephosphate isomerase deficiency   44641000
  • Overhydrated hereditary stomatocytosis   722125003
  • Phosphoglycerokinase deficiency   234403002
  • Southeast Asian ovalocytosis   723623002
  • Triose phosphate isomerase deficiency   234405009
  • Uridine monophosphate hydrolase deficiency   234407001
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Red blood cell disorder   38292009
          Erythrocyte enzyme deficiency   234401000

ancestors
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