ValueSet-2.16.840.1.113762.1.4.1078.490

Sourceus.nlm.vsac#0.11.0:null (v4.0.1)
resourceTypeValueSet
id2.16.840.1.113762.1.4.1078.490
canonicalhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1078.490
version20230601
statusactive
publisherOptum Steward
nameComplementDeficiencies
titleComplement Deficiencies
date2023-06-01T01:01:19-04:00
descriptionSCT codes for Complement deficiencies
Usages(none)

This value set contains 47 concepts

Code System Display
   1162263002 http://snomed.info/sct Complement component 8 deficiency (disorder)
   18827005 http://snomed.info/sct Complement abnormality (disorder)
   234593008 http://snomed.info/sct Classical complement pathway abnormality (disorder)
   234594002 http://snomed.info/sct Complement 1q deficiency (disorder)
   234595001 http://snomed.info/sct Complement 1q beta chain deficiency (disorder)
   234596000 http://snomed.info/sct Complement 1q dysfunction (disorder)
   234597009 http://snomed.info/sct Complement 1r deficiency (disorder)
   234598004 http://snomed.info/sct Complement 1s deficiency (disorder)
   234599007 http://snomed.info/sct Complement 2 deficiency (disorder)
   234600005 http://snomed.info/sct Complement 4 deficiency (disorder)
   234601009 http://snomed.info/sct Complement 4A deficiency (disorder)
   234602002 http://snomed.info/sct Complement 4B deficiency (disorder)
   234604001 http://snomed.info/sct Alternative pathway deficiency (disorder)
   234605000 http://snomed.info/sct Factor B deficiency (disorder)
   234607008 http://snomed.info/sct Factor D deficiency (disorder)
   234608003 http://snomed.info/sct Terminal component deficiency (disorder)
   234609006 http://snomed.info/sct Complement 5 deficiency (disorder)
   234611002 http://snomed.info/sct Complement 6 deficiency (disorder)
   234612009 http://snomed.info/sct Complement 7 deficiency (disorder)
   234613004 http://snomed.info/sct Combined complement 6 and 7 deficiencies (disorder)
   234614005 http://snomed.info/sct Complement 8 beta chain deficiency (disorder)
   234615006 http://snomed.info/sct Complement 8 beta chain dysfunction (disorder)
   234616007 http://snomed.info/sct Complement 8 alpha-gamma deficiency (disorder)
   234617003 http://snomed.info/sct Complement 9 deficiency (disorder)
   234618008 http://snomed.info/sct Complement regulatory factor defect (disorder)
   234619000 http://snomed.info/sct Hereditary C1 esterase inhibitor deficiency - deficient factor (disorder)
   234620006 http://snomed.info/sct Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder)
   234621005 http://snomed.info/sct Factor I deficiency (disorder)
   234622003 http://snomed.info/sct Factor H deficiency (disorder)
   234623008 http://snomed.info/sct Complement 4 binding protein deficiency (disorder)
   234624002 http://snomed.info/sct Decay accelerating factor deficiency (disorder)
   234625001 http://snomed.info/sct Homologous restriction factor deficiency (disorder)
   234626000 http://snomed.info/sct Complement 5a inhibitor deficiency (disorder)
   234627009 http://snomed.info/sct Anaphylotoxin inactivator deficiency (disorder)
   234628004 http://snomed.info/sct Complement receptor deficiency (disorder)
   234629007 http://snomed.info/sct Complement receptor 1 deficiency (disorder)
   234630002 http://snomed.info/sct Complement receptor 3 deficiency (disorder)
   24419001 http://snomed.info/sct Disorder of complement (disorder)
   24743004 http://snomed.info/sct Complement deficiency disease (disorder)
   263661007 http://snomed.info/sct Complement 5 dysfunction (disorder)
   39674000 http://snomed.info/sct Familial C3B inhibitor deficiency syndrome (disorder)
   771078002 http://snomed.info/sct Immunodeficiency due to mannan binding lectin serine peptidase 2 deficiency (disorder)
   771443008 http://snomed.info/sct Complement component 3 deficiency (disorder)
   778027003 http://snomed.info/sct Primary CD59 deficiency (disorder)
   783007005 http://snomed.info/sct Recurrent Neisseria infection due to factor D deficiency (disorder)
   783621008 http://snomed.info/sct Immunodeficiency with factor I anomaly (disorder)
   81166004 http://snomed.info/sct Properdin deficiency disease (disorder)

Produced 08 Sep 2023