ValueSet-2.16.840.1.113762.1.4.1146.2105

Sourceus.nlm.vsac#0.11.0:null (v4.0.1)
resourceTypeValueSet
id2.16.840.1.113762.1.4.1146.2105
canonicalhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2105
version20230125
statusactive
publisherCSTE Steward
nameMethemoglobinemiaDisordersSNOMED
titleMethemoglobinemia (Disorders) (SNOMED)
date2023-01-25T01:08:07-05:00
Usages(none)

This value set contains 16 concepts

Code System Display
   127037003 http://snomed.info/sct Toxic methemoglobinemia with cyanosis (disorder)
   131171006 http://snomed.info/sct Methemoglobin above reference range (finding)
   191388008 http://snomed.info/sct Familial methemoglobinemia (disorder)
   191389000 http://snomed.info/sct Idiopathic methemoglobinemia (disorder)
   191390009 http://snomed.info/sct Drug-induced methemoglobinemia (disorder)
   234395000 http://snomed.info/sct Congenital methemoglobinaema with defective methemoglobin-reducing system (disorder)
   234396004 http://snomed.info/sct Congenital methemoglobinemia with abnormal methemoglobins (disorder)
   267550008 http://snomed.info/sct Congenital methemoglobinemia (disorder)
   295315008 http://snomed.info/sct Acquired methemoglobinemia (disorder)
   38959009 http://snomed.info/sct Methemoglobinemia (disorder)
   406593009 http://snomed.info/sct Methemoglobinemia caused by nitrate poisoning (disorder)
   57020009 http://snomed.info/sct Stokvis' disease (disorder)
   74912001 http://snomed.info/sct Hereditary methemoglobinemia due to globin chain mutation (disorder)
   767497003 http://snomed.info/sct Autosomal recessive congenital methemoglobinemia (disorder)
   767498008 http://snomed.info/sct Autosomal recessive congenital methemoglobinemia type II (disorder)
   767499000 http://snomed.info/sct Autosomal recessive congenital methemoglobinemia type I (disorder)

Produced 08 Sep 2023