OMOP Concept 4264017

Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia

StandardConditionSNOMED61395005Disorder
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 Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia across source vocabularies.

  • Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
  • Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder)
  • HPFH (hereditary persistence of fetal haemoglobin) G gamma beta plus thalassaemia
  • HPFH (hereditary persistence of fetal hemoglobin) G gamma beta plus thalassemia
  • HPFH (hereditary persistence of foetal haemoglobin) G gamma beta plus thalassaemia
  • talasemia por persistencia hereditaria de hemoglobina fetal gamma beta más
  • talasemia por persistencia hereditaria de hemoglobina fetal gamma beta más (trastorno)

Where it sits in the hierarchy

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

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