Hereditary nonspherocytic hemolytic anemia   301317008

SNOMED CT code


SNOMED code301317008
nameHereditary nonspherocytic hemolytic anemia
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary nonspherocytic hemolytic anemia (disorder)
synonyms
  • Hereditary nonspherocytic haemolytic anaemia
  • Congenital nonspherocytic hemolytic anemia
  • Hereditary nonspherocytic hemolytic anemia
  • Congenital nonspherocytic haemolytic anaemia
  • HNSHA - hereditary nonspherocytic hemolytic anemia
  • HNSHA - hereditary nonspherocytic haemolytic anaemia
attributes - group3
Has interpretationPresent   52101004
InterpretsHemolysis   404227002
attributes - group4
Finding siteErythrocyte   41898006
attributes - group1
Has interpretationBelow reference range   281300000
InterpretsMeasurement of total hemoglobin concentration   441689006
attributes - group2
Has interpretationBelow reference range   281300000
InterpretsRed blood cell count   14089001
parentsHereditary hemolytic anemia   38911009
children
  • Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism   363041004
  • Hemolytic anemia due to adenylate kinase deficiency   766982000
  • Hemolytic anemia due to erythrocyte adenosine deaminase overproduction   5315003
  • HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency   74703006
  • 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 glucose phosphate isomerase deficiency   52413004
  • HNSHA due to glutathione reductase deficiency   52212006
  • 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
  • Lethal hemolytic anemia and genital anomaly syndrome   719402008
  • Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase   725057008
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
          Hereditary red blood cell disorder   414394009
            Hereditary hemolytic anemia   38911009
              Hereditary nonspherocytic hemolytic anemia   301317008

ancestors
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