OMOP Concept 4156027

Hereditary hypertyrosinemia

StandardConditionSNOMED271847005Disorder
Maps from
3
Descendants
3
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept

3 source codes normalize to Hereditary hypertyrosinemia via the OMOP "Maps to" relationship.

VocabularyCodeNameType
CIEL138766Hereditary HypertyrosinemiaNon-standard
MeSHD020176TyrosinemiasNon-standard
Nebraska Lexicon271847005Tyrosinaemia-tyrosiluria hereditary syndromeNon-standard

Synonyms

Alternative names recorded for Hereditary hypertyrosinemia across source vocabularies.

  • Hereditary hypertyrosinaemia
  • Hereditary hypertyrosinemia (disorder)
  • Hereditary tyrosinaemia
  • Hereditary tyrosinemia
  • hipertirosinemia hereditaria
  • hipertirosinemia hereditaria (trastorno)
  • síndrome de tirosinemia-tirosinuria hereditaria
  • Tyrosinaemia-tyrosiluria hereditary syndrome
  • Tyrosinemia-tyrosiluria hereditary syndrome

Where it sits in the hierarchy

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

Broader concepts

(14)

Roll up to these when you need a wider cohort.

Narrower concepts

(3)

Included automatically when you query with descendants.

Get this concept via the API

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