SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Lissencephaly with cerebellar hypoplasia  715817007

Lissencephaly with cerebellar hypoplasia type B   715819005

SNOMED CT code


SNOMED code715819005
nameLissencephaly with cerebellar hypoplasia type B
statusactive
date introduced2016-07-31
fully specified name(s)Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder)
synonyms
  • Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B
  • Lissencephaly with cerebellar hypoplasia type B
attributes - group1
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Associated morphologyHypoplasia   55199003
Finding siteCerebellar structure   113305005
parentsLissencephaly with cerebellar hypoplasia   715817007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Lissencephaly with cerebellar hypoplasia   715817007
          Lissencephaly with cerebellar hypoplasia type B   715819005

ancestors
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