SNOMED CT Concept  138875005

Clinical finding  404684003

Functional finding  118228005

Mucociliary clearance defect  233660001

Inherited mucociliary clearance defect   233661002

SNOMED CT code


SNOMED code233661002
nameInherited mucociliary clearance defect
statusactive
date introduced2002-01-31
fully specified name(s)Inherited mucociliary clearance defect (disorder)
synonyms
  • Inherited mucociliary clearance defect
  • Inherited impaired mucociliary clearance
  • Inherited defective mucociliary clearance
attributes - group1
Has interpretationImpaired   260379002
InterpretsMucociliary clearance   63533009
attributes - group2
Finding siteRespiratory tract structure   321667001
parents
children
  • Cystic fibrosis   190905008
  • Immotile cilia syndrome   86204009
  • Immotile cilia syndrome due to excessively long cilia   233665006
  • Primary ciliary dyskinesia and retinitis pigmentosa syndrome   719282008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Mucociliary clearance defect   233660001
        Inherited mucociliary clearance defect   233661002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Hereditary disorder by system   363137000
          Inherited mucociliary clearance defect   233661002

ancestors
sorted most to least specific
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