230561007: Congenital neuropathy with arthrogryposis multiplex congenita (disorder)

• SNOMED CT Concept\constatation clinique\...
• \Deformity (finding)\anomalie morphologique congénitale\Arthrogryposis\Congenital neuropathy with arthrogryposis multiplex congenita
• \Deformity (finding)\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Congenital neuropathy with arthrogryposis multiplex congenita
• \constatation à propos du mouvement\constatation à propos du mouvement de l'articulation\Finding of range of joint movement\Limitation of joint movement\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Congenital neuropathy with arthrogryposis multiplex congenita
• \constatation à propos du mouvement\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Congenital neuropathy with arthrogryposis multiplex congenita
• \Disease\Disorder of joint region\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Congenital neuropathy with arthrogryposis multiplex congenita
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Neuropathy (disorder)\Congenital neuropathy with arthrogryposis multiplex congenita
• \Disease\Congenital disease\Congenital malformation\anomalie morphologique congénitale\Arthrogryposis\Congenital neuropathy with arthrogryposis multiplex congenita
• \Disease\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Congenital neuropathy with arthrogryposis multiplex congenita
• \Disease\trouble du développement\Congenital malformation\anomalie morphologique congénitale\Arthrogryposis\Congenital neuropathy with arthrogryposis multiplex congenita

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
345473013	Congenital neuropathy with arthrogryposis multiplex congenita	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
618388015	Congenital neuropathy with arthrogryposis multiplex congenita (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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