SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Hereditary hemoglobinopathy  427306008

Hereditary hemoglobinopathy due to globin chain mutation  127038008

Congenital methemoglobinemia with abnormal methemoglobins   234396004

SNOMED CT code


SNOMED code234396004
nameCongenital methemoglobinemia with abnormal methemoglobins
statusactive
date introduced2002-01-31
fully specified name(s)Congenital methemoglobinemia with abnormal methemoglobins (disorder)
synonyms
  • Congenital methemoglobinemia with abnormal methemoglobins
  • Congenital methaemoglobinaemia with abnormal methaemoglobins
attributes - group1
OccurrenceCongenital   255399007
Finding siteErythrocyte   41898006
parents
  • Hereditary hemoglobinopathy due to globin chain mutation   127038008
  • Congenital methemoglobinemia   267550008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary hemoglobinopathy   427306008
          Hereditary hemoglobinopathy due to globin chain mutation   127038008
            Congenital methemoglobinemia with abnormal methemoglobins   234396004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital methemoglobinemia   267550008
          Congenital methemoglobinemia with abnormal methemoglobins   234396004

ancestors
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