Congenital neuropathy with arthrogryposis multiplex congenita   230561007

SNOMED CT code


SNOMED code230561007
nameCongenital neuropathy with arthrogryposis multiplex congenita
statusactive
date introduced2002-01-31
fully specified name(s)Congenital neuropathy with arthrogryposis multiplex congenita (disorder)
synonymsCongenital neuropathy with arthrogryposis multiplex congenita
attributes - group1
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Finding siteNerve structure   3057000
attributes - group2
Pathological processPathological developmental process   308490002
Finding siteStructure of joint region   785818007
OccurrenceCongenital   255399007
Associated morphologyContracture   57048009
attributes - group3
InterpretsRange of joint movement   364564000
Has interpretationDecreased   1250004
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Deformity   417893002
      Congenital deformity   276655000
        Arthrogryposis   111246005
          Congenital neuropathy with arthrogryposis multiplex congenita   230561007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Disorder by body site   123946008
        Disorder of body system   362965005
          Disorder of nervous system   118940003
            Neuropathy   386033004
              Congenital neuropathy with arthrogryposis multiplex congenita   230561007

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