Porencephaly, cerebellar hypoplasia, internal malformations syndrome   763821001

SNOMED CT code


SNOMED code763821001
namePorencephaly, cerebellar hypoplasia, internal malformations syndrome
statusactive
date introduced2018-07-31
fully specified name(s)Porencephaly, cerebellar hypoplasia, internal malformations syndrome (disorder)
synonyms
  • Porencephaly, cerebellar hypoplasia, internal malformations syndrome
  • Bonnemann Meinecke syndrome
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyCystic dilatation   125269003
OccurrenceCongenital   255399007
Finding siteBrain structure   12738006
attributes - group3
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Associated morphologyHypoplasia   55199003
Finding siteCerebellar structure   113305005
attributes - group2
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Associated morphologyAbsence   418560003
Finding siteCerebellar vermis structure   58501004
parents
  • Congenital cerebellar hypoplasia   16026008
  • Absence of the vermis   253177006
  • Congenital absence of part of brain   26595007
  • Congenital porencephaly   38353004
  • Multiple system malformation syndrome   82354003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Finding of brain   299718000
        Disorder of brain   81308009
          Cerebellar disorder   223176004
            Dysgenesis of the cerebellum   253171007
              Congenital cerebellar hypoplasia   16026008
                Porencephaly, cerebellar hypoplasia, internal malformations syndrome   763821001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Finding of brain   299718000
        Disorder of brain   81308009
          Cerebellar disorder   223176004
            Absence of the vermis   253177006
              Porencephaly, cerebellar hypoplasia, internal malformations syndrome   763821001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Disorder of the central nervous system   23853001
        Congenital anomaly of central nervous system   128124001
          Congenital anomaly of brain   57148006
            Anencephalus   89369001
              Congenital absence of part of brain   26595007
                Porencephaly, cerebellar hypoplasia, internal malformations syndrome   763821001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Neurological lesion   299735001
      Lesion of brain   301766008
        Congenital porencephaly   38353004
          Porencephaly, cerebellar hypoplasia, internal malformations syndrome   763821001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Multiple system malformation syndrome   82354003
              Porencephaly, cerebellar hypoplasia, internal malformations syndrome   763821001

ancestors
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