OMOP Concept 36715328

Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3

StandardConditionSNOMED720951008Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
OMOP concepts

Concept Lookup Tool

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

Source codes that map to this concept

1 source code normalizes to Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 across source vocabularies.

  • Combined oxidative phosphorylation deficiency type 3
  • deficiencia combinada de la fosforilación oxidativa tipo 3
  • enfermedad mitocondrial fatal debida a deficiencia combinada de la fosforilación oxidativa 3
  • enfermedad mitocondrial fatal debida a deficiencia combinada de la fosforilación oxidativa 3 (trastorno)
  • Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (disorder)

Where it sits in the hierarchy

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

Get this concept via the API

Resolve Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 - 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/36715328?include_relationships=true" \
  -H "Authorization: Bearer $OMOPHUB_API_KEY"
Get your free API key3,000 calls/month free · no credit card