Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome   783156008

SNOMED CT code


SNOMED code783156008
nameFibular aplasia, tibial campomelia, oligo-syndactyly syndrome
statusactive
date introduced2019-07-31
fully specified name(s)Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome (disorder)
synonyms
  • Hecht Scott syndrome
  • FATCO syndrome
  • Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome
attributes - group1
Associated morphologyAbnormal shortening   45056002
OccurrenceCongenital   255399007
Finding siteEntire limb   243996003
Pathological processPathological developmental process   308490002
parents
  • Multiple malformation syndrome with limb defect as major feature   41443008
  • Longitudinal deficiency of limb   67341007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Multiple system malformation syndrome   82354003
              Multiple malformation syndrome with limb defect as major feature   41443008
                Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome   783156008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Deformity of limb   445144002
        Longitudinal deficiency of limb   67341007
          Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome   783156008

ancestors
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