OMOP Concept 37204850

Autosomal recessive hyperinsulinism due to Kir6.2 deficiency

StandardConditionSNOMED783768006Disorder
Maps from
0
Descendants
0
Valid from
31 Jul 2019
Valid to
31 Dec 2099
OMOP concepts

Concept Lookup Tool

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

Or try
DiabetesHypertensionAspirin

Synonyms

Alternative names recorded for Autosomal recessive hyperinsulinism due to Kir6.2 deficiency across source vocabularies.

  • Autosomal recessive hyperinsulinemic hypoglycaemia due to Kir6.2 deficiency
  • Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency
  • Autosomal recessive hyperinsulinism due to Kir6.2 deficiency (disorder)
  • hiperinsulinismo autosómico recesivo debido a deficiencia de Kir6.2
  • hiperinsulinismo autosómico recesivo debido a deficiencia de Kir6.2 (trastorno)

Where it sits in the hierarchy

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

Broader concepts

(37)

Roll up to these when you need a wider cohort.

Showing 25 of 37. Retrieve the full set via the API.

Get this concept via the API

Resolve Autosomal recessive hyperinsulinism due to Kir6.2 deficiency - 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/37204850?include_relationships=true" \
  -H "Authorization: Bearer $OMOPHUB_API_KEY"
Get your free API key3,000 calls/month free · no credit card