Cardiocranial syndrome Pfeiffer type   720606005

SNOMED CT code


SNOMED code720606005
nameCardiocranial syndrome Pfeiffer type
statusactive
date introduced2017-01-31
fully specified name(s)Cardiocranial syndrome Pfeiffer type (disorder)
synonyms
  • Cardiocranial syndrome Pfeiffer type
  • Craniosynostosis with congenital heart disease and intellectual disability syndrome
  • Pfeiffer Singer Zschiesche syndrome
  • Sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteStructure of sagittal suture of skull   62169003
Associated morphologyCongenital premature fusion   67798003
attributes - group2
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
Finding siteHeart structure   80891009
parents
  • Congenital heart disease   13213009
  • Developmental delay   248290002
  • Cardiovascular system hereditary disorder   363005004
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of musculoskeletal system   363212003
  • Craniosynostosis syndrome   57219006
  • Multiple system malformation syndrome   82354003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Cardiac finding   301095005
        Heart disease   56265001
          Structural disorder of heart   128599005
            Congenital heart disease   13213009
              Cardiocranial syndrome Pfeiffer type   720606005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental delay   248290002
          Cardiocranial syndrome Pfeiffer type   720606005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Disorder of cardiovascular system   49601007
        Cardiovascular system hereditary disorder   363005004
          Cardiocranial syndrome Pfeiffer type   720606005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Cardiocranial syndrome Pfeiffer type   720606005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Cardiocranial syndrome Pfeiffer type   720606005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Joint finding   118952005
        Cranial suture finding   248387005
          Imperfect fusion of skull   23939000
            Craniosynostosis syndrome   57219006
              Cardiocranial syndrome Pfeiffer type   720606005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Multiple system malformation syndrome   82354003
              Cardiocranial syndrome Pfeiffer type   720606005

ancestors
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