OMOP Concept 604334

Alpha-N-acetylgalactosaminidase deficiency type 1

StandardConditionSNOMED879937000Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2021
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

1 source code normalizes to Alpha-N-acetylgalactosaminidase deficiency type 1 via the OMOP "Maps to" relationship.

VocabularyCodeNameType
MeSHC536631Schindler Disease, Type INon-standard

Synonyms

Alternative names recorded for Alpha-N-acetylgalactosaminidase deficiency type 1 across source vocabularies.

  • Alpha-N-acetylgalactosaminidase deficiency type 1 (disorder)
  • deficiencia de alfa-N-acetilgalactosaminidasa tipo 1
  • deficiencia de alfa-N-acetilgalactosaminidasa tipo 1 (trastorno)
  • deficiencia de NAGA (alfa-N-acetilgalactosaminidasa) tipo 1
  • enfermedad de Schindler tipo 1
  • NAGA (alpha-N-acetylgalactosaminidase) deficiency type 1
  • Schindler disease type 1

Where it sits in the hierarchy

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

Broader concepts

(23)

Roll up to these when you need a wider cohort.

Get this concept via the API

Resolve Alpha-N-acetylgalactosaminidase deficiency type 1 - 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/604334?include_relationships=true" \
  -H "Authorization: Bearer $OMOPHUB_API_KEY"
Get your free API key3,000 calls/month free · no credit card