de Barsey syndrome   59252009

SNOMED CT code


SNOMED code59252009
namede Barsey syndrome
statusactive
date introduced2002-01-31
fully specified name(s)de Barsey syndrome (disorder)
synonyms
  • Autosomal recessive cutis laxa type III
  • Cutis laxa-corneal clouding-oligophrenia syndrome
  • de Barsey syndrome
  • Progeroid syndrome of de Barsey
  • de Barsey-Moens-Dierckx syndrome
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteCorneal structure   28726007
Associated morphologyOpacity   128305008
attributes - group2
Finding siteFace structure   89545001
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
attributes - group3
OccurrenceCongenital   255399007
Finding siteConnective tissue structure   21793004
Pathological processPathological developmental process   308490002
attributes - group4
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Finding siteSkin structure   39937001
attributes - group5
Finding siteJoint structure   39352004
attributes - group6
InterpretsReflex   87572000
Has interpretationAbnormal   263654008
attributes - group7
InterpretsIntellectual ability   247573007
Has interpretationImpaired   260379002
attributes - group8
InterpretsAdaptation behavior   406208005
Has interpretationImpaired   260379002
parents
  • Intellectual disability   110359009
  • Developmental delay   248290002
  • Congenital corneal opacity   268160006
  • Joint laxity   298203008
  • Musculoskeletal and connective tissue disorder   312225001
  • Hereditary disorder of musculoskeletal system   363212003
  • Hereditary disorder of the visual system   363343008
  • Disorder of proline AND/OR hydroxyproline metabolism   37800003
  • Arthropathy   399269003
  • Athetoid movement   58593005
  • Cutis laxa, autosomal recessive   59451000
  • Multiple malformation syndrome with facial defects as major feature   65094009
  • Hyperreflexia   86854008
children
  • ALDH18A1-related de Barsy syndrome   1295485009
  • Pyrroline-5-carboxylate reductase 1 related de Barsy syndrome   1295488006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Mental state, behavior and/or psychosocial function finding   384821006
      Behavior finding   844005
        Intellectual disability   110359009
          de Barsey syndrome   59252009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental delay   248290002
          de Barsey syndrome   59252009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Degenerative disorder of eye   62585004
          Corneal degeneration   111521006
            Corneal opacity   64634000
              Congenital corneal opacity   268160006
                de Barsey syndrome   59252009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Joint finding   118952005
        Joint laxity   298203008
          de Barsey syndrome   59252009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of connective tissue   105969002
        Musculoskeletal and connective tissue disorder   312225001
          de Barsey syndrome   59252009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          de Barsey syndrome   59252009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Hereditary disorder of the visual system   363343008
          de Barsey syndrome   59252009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of organic acid metabolism   116021002
          Disorder of amino acid metabolism   44779003
            Disorder of amino acid and organic acid metabolism   237911005
              Disorder of proline AND/OR hydroxyproline metabolism   37800003
                de Barsey syndrome   59252009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Joint finding   118952005
        Arthropathy   399269003
          de Barsey syndrome   59252009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of coordination   298314008
      Athetoid movement   58593005
        de Barsey syndrome   59252009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of connective tissue   105969002
        Congenital connective tissue disorder   363039000
          Inherited cutis laxa   254220005
            Cutis laxa, autosomal recessive   59451000
              de Barsey syndrome   59252009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of head   118934005
        Disorder of face   118930001
          Congenital anomaly of face   398302004
            Multiple malformation syndrome with facial defects as major feature   65094009
              de Barsey syndrome   59252009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Neurological finding   102957003
      Reflex finding   106146005
        Abnormal reflex   46670006
          Hyperreflexia   86854008
            de Barsey syndrome   59252009

ancestors
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