OMOP Concept 4142629

Hereditary factor II deficiency disease

StandardConditionSNOMED33297000Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts

Concept Lookup Tool

Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.

Or try
DiabetesHypertensionAspirin

Source codes that map to this concept

2 source codes normalize to Hereditary factor II deficiency disease via the OMOP "Maps to" relationship.

VocabularyCodeNameType
CIEL138777Hereditary Factor II deficiency diseaseNon-standard
MeSHC562724DysprothrombinemiaNon-standard

Synonyms

Alternative names recorded for Hereditary factor II deficiency disease across source vocabularies.

  • deficiencia hereditaria de factor II
  • deficiencia hereditaria de factor II (trastorno)
  • Hereditary factor II deficiency disease (disorder)
  • Hereditary hypoprothrombinaemia
  • Hereditary hypoprothrombinemia
  • hipoprotrombinemia hereditaria

Where it sits in the hierarchy

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

Broader concepts

(24)

Roll up to these when you need a wider cohort.

Get this concept via the API

Resolve Hereditary factor II deficiency disease - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.

curl "https://api.omophub.com/v1/concepts/4142629?include_relationships=true" \
  -H "Authorization: Bearer $OMOPHUB_API_KEY"
Get your free API key3,000 calls/month free · no credit card