77016009: Amyoplasia congenita disruptive sequence (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Deformity\Congenital deformity\Arthrogryposis\Amyoplasia congenita disruptive sequence
• \Deformity\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Amyoplasia congenita disruptive sequence
• \Finding of movement\Finding of joint movement\Finding of range of joint movement\Limitation of joint movement\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Amyoplasia congenita disruptive sequence
• \Finding of movement\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Amyoplasia congenita disruptive sequence
• \Disease\Disorder of joint region\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Amyoplasia congenita disruptive sequence
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with unusual brain and/or neuromuscular findings\Amyoplasia congenita disruptive sequence
• \Disease\Congenital disease\Congenital anomaly\Congenital deformity\Arthrogryposis\Amyoplasia congenita disruptive sequence
• \Disease\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Amyoplasia congenita disruptive sequence
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with unusual brain and/or neuromuscular findings\Amyoplasia congenita disruptive sequence
• \Disease\Developmental disorder\Congenital anomaly\Congenital deformity\Arthrogryposis\Amyoplasia congenita disruptive sequence

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
127855010	Amyoplasia congenita disruptive sequence	en	Synonym	Active	Case insensitive	SNOMED CT core
127856011	Myodystrophia foetalis deformans	en	Synonym	Active	Case insensitive	SNOMED CT core
127857019	Classic arthrogryposis	en	Synonym	Active	Case insensitive	SNOMED CT core
127858012	Arthrogryposis multiplex congenita	en	Synonym	Inactive	Case insensitive	SNOMED CT core
127859016	Myodystrophia fetalis deformans	en	Synonym	Active	Case insensitive	SNOMED CT core
127860014	Multiple congenital articular rigidities	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
127861013	Congenital arthromyodysplasia	en	Synonym	Active	Case insensitive	SNOMED CT core
127862018	Myophagism congenita	en	Synonym	Active	Case insensitive	SNOMED CT core
127863011	Amyoplasia congenita	en	Synonym	Active	Case insensitive	SNOMED CT core
127864017	Congenital multiple arthrogryposis	en	Synonym	Inactive	Case insensitive	SNOMED CT core
503436016	AMC - Arthrogryposis multiplex congenita	en	Synonym	Inactive	Case sensitive	SNOMED CT core
816381000036112	Myodystrophia foetalis deformans	en	Synonym	Inactive	Initial character case insensitive	SNOMED Clinical Terms Australian extension
817800016	Amyoplasia congenita disruptive sequence (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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