Amyoplasia congenita disruptive sequence   77016009

SNOMED CT code


SNOMED code77016009
nameAmyoplasia congenita disruptive sequence
statusremoved
date introduced2002-01-31
fully specified name(s)Amyoplasia congenita disruptive sequence (disorder)
synonyms
  • Amyoplasia congenita disruptive sequence
  • Myodystrophia foetalis deformans
  • Classic arthrogryposis
  • Myodystrophia fetalis deformans
  • Congenital arthromyodysplasia
  • Myophagism congenita
  • Amyoplasia congenita
parentsCongenital anomaly of joint   95463009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Joint finding   118952005
        Arthropathy   399269003
          Congenital anomaly of joint   95463009
            Amyoplasia congenita disruptive sequence   77016009  removed: 2023-02-28

ancestors
sorted most to least specific
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