ValueSet-2.16.840.1.113762.1.4.1146.2140

Sourceus.nlm.vsac#0.11.0:null (v4.0.1)
resourceTypeValueSet
id2.16.840.1.113762.1.4.1146.2140
canonicalhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1146.2140
version20230122
statusactive
publisherCSTE Steward
namePhenylketonuriaDisordersSNOMED
titlePhenylketonuria (Disorders) (SNOMED)
date2023-01-22T01:03:33-05:00
Usages(none)

This value set contains 9 concepts

Code System Display
   1003938005 http://snomed.info/sct Phenylketonuria due to tetrahydrobiopterin deficiency (disorder)
   190687004 http://snomed.info/sct Phenylketonuria (disorder)
   297225000 http://snomed.info/sct Maternal phenylketonuria (disorder)
   40751003 http://snomed.info/sct Persistent hyperphenylalaninemia AND tyrosinemia (disorder)
   440009 http://snomed.info/sct Persistent hyperphenylalaninemia (disorder)
   60590005 http://snomed.info/sct Maternal phenylketonuria fetal effect (disorder)
   7573000 http://snomed.info/sct Classical phenylketonuria (disorder)
   890435004 http://snomed.info/sct Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase (disorder)
   890436003 http://snomed.info/sct Classical phenylketonuria with total deficiency of phenylalanine hydroxylase (disorder)

Produced 08 Sep 2023