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Terminology chevron_right Concepts chevron_right 77016009

Production
The component that hold information about this concept.
Amyoplasia congenita disruptive sequence (disorder)
Amyoplasia congenita
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Amyoplasia congenita disruptive sequence (disorder)

SCTID: 77016009, Primitive, Inactive


77016009|Amyoplasia congenita disruptive sequence (disorder)|
  • en Amyoplasia congenita
  • en Amyoplasia congenita disruptive sequence
  • en Amyoplasia congenita disruptive sequence (disorder)
  • en Classic arthrogryposis
  • en Congenital arthromyodysplasia
  • en Myodystrophia fetalis deformans
  • en Myodystrophia foetalis deformans
  • en Myophagism congenita

77016009 |Amyoplasia congenita disruptive sequence (disorder)|

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