OMOP Concept 4258685

HNSHA due to triosephosphate isomerase deficiency

StandardConditionSNOMED44641000Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept

2 source codes normalize to HNSHA due to triosephosphate isomerase deficiency via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for HNSHA due to triosephosphate isomerase deficiency across source vocabularies.

  • anemia hemolítica no esferocítica hereditaria por deficiencia de triosafosfato isomerasa
  • anemia hemolítica no esferocítica hereditaria por deficiencia de triosafosfato isomerasa (trastorno)
  • Hereditary nonspherocytic haemolytic anaemia due to triosephosphate isomerase deficiency
  • Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to triosephosphate isomerase deficiency
  • Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency
  • Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder)
  • Hereditary nonspherocytic hemolytic anemia (HNSHA) due to triosephosphate isomerase deficiency
  • Triosephosphate deficiency anaemia
  • Triosephosphate deficiency anemia

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

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