SNOMED CT Concept  138875005

Clinical finding  404684003

Finding of blood, lymphatics and immune system  299691001

Disorder of cellular component of blood  414022008

Hemolytic disorder  128086004

Hemolytic anemia  61261009

Anemia due to enzyme deficiency  111577008

HNSHA due to NADH diaphorase deficiency   47526003

SNOMED CT code


SNOMED code47526003
nameHNSHA due to NADH diaphorase deficiency
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder)
synonyms
  • Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH) diaphorase deficiency
  • Hereditary nonspherocytic hemolytic anemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH) diaphorase deficiency
  • Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency
  • Hereditary nonspherocytic haemolytic anaemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency
  • HNSHA due to NADH diaphorase deficiency
attributes - group3
Has interpretationPresent   52101004
InterpretsHemolysis   404227002
attributes - group6
Due toEnzymopathy   78548001
attributes - group1
Has interpretationBelow reference range   281300000
InterpretsRed blood cell count   14089001
attributes - group2
Has interpretationBelow reference range   281300000
InterpretsMeasurement of total hemoglobin concentration   441689006
attributes - group4
Finding siteErythrocyte   41898006
attributes - group5
OccurrenceCongenital   255399007
parents
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
        Hemolytic disorder   128086004
          Hemolytic anemia   61261009
            Anemia due to enzyme deficiency   111577008
              HNSHA due to NADH diaphorase deficiency   47526003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Red blood cell disorder   38292009
          Erythrocyte enzyme deficiency   234401000
            HNSHA due to NADH diaphorase deficiency   47526003

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
                HNSHA due to NADH diaphorase deficiency   47526003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital anemia   63565007
          HNSHA due to NADH diaphorase deficiency   47526003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          HNSHA due to NADH diaphorase deficiency   47526003

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