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715316005: Neurogenic arthrogryposis multiplex congenita (disorder)

SNOMED CT Concept\Clinical finding\...

\Deformity\Congenital deformity\Arthrogryposis\Inherited arthrogryposis\Neurogenic arthrogryposis multiplex congenita
\Deformity\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Inherited arthrogryposis\Neurogenic arthrogryposis multiplex congenita

\Finding of movement\Finding of joint movement\Finding of range of joint movement\Joint movement absent\Neurogenic arthrogryposis multiplex congenita
\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\Inherited arthrogryposis\Neurogenic arthrogryposis multiplex congenita
\Finding of movement\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Inherited arthrogryposis\Neurogenic arthrogryposis multiplex congenita

\Disease\Disorder of joint region\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Inherited arthrogryposis\Neurogenic arthrogryposis multiplex congenita
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Inherited arthrogryposis\Neurogenic arthrogryposis multiplex congenita
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Neurogenic arthrogryposis multiplex congenita
\Disease\Congenital disease\Congenital malformation\Congenital deformity\Arthrogryposis\Inherited arthrogryposis\Neurogenic arthrogryposis multiplex congenita
\Disease\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Inherited arthrogryposis\Neurogenic arthrogryposis multiplex congenita
\Disease\Developmental disorder\Developmental hereditary disorder\Inherited arthrogryposis\Neurogenic arthrogryposis multiplex congenita
\Disease\Developmental disorder\Congenital malformation\Congenital deformity\Arthrogryposis\Inherited arthrogryposis\Neurogenic arthrogryposis multiplex congenita

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3302194018 Neurogenic arthrogryposis multiplex congenita (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3302195017 Neurogenic arthrogryposis multiplex congenita en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Neurogenic arthrogryposis multiplex congenita	Due to	Denervation atrophy of muscle	true	Inferred relationship	Existential restriction modifier	3
Neurogenic arthrogryposis multiplex congenita	Is a	Arthropathy associated with another disorder	false	Inferred relationship	Existential restriction modifier
Neurogenic arthrogryposis multiplex congenita	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Neurogenic arthrogryposis multiplex congenita	Is a	Arthrogryposis	false	Inferred relationship	Existential restriction modifier
Neurogenic arthrogryposis multiplex congenita	Is a	Hereditary disorder of musculoskeletal system	false	Inferred relationship	Existential restriction modifier
Neurogenic arthrogryposis multiplex congenita	Associated morphology	Contracture	false	Inferred relationship	Existential restriction modifier	2
Neurogenic arthrogryposis multiplex congenita	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Neurogenic arthrogryposis multiplex congenita	Finding site	Joint structure	false	Inferred relationship	Existential restriction modifier	2
Neurogenic arthrogryposis multiplex congenita	Associated morphology	Contracture	true	Inferred relationship	Existential restriction modifier	1
Neurogenic arthrogryposis multiplex congenita	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Neurogenic arthrogryposis multiplex congenita	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Neurogenic arthrogryposis multiplex congenita	Interprets	Range of joint movement	true	Inferred relationship	Existential restriction modifier	2
Neurogenic arthrogryposis multiplex congenita	Finding site	Structure of joint region	true	Inferred relationship	Existential restriction modifier	1
Neurogenic arthrogryposis multiplex congenita	Has interpretation	Absent	true	Inferred relationship	Existential restriction modifier	2
Neurogenic arthrogryposis multiplex congenita	Is a	Joint movement absent	true	Inferred relationship	Existential restriction modifier
Neurogenic arthrogryposis multiplex congenita	Is a	Inherited arthrogryposis	true	Inferred relationship	Existential restriction modifier
Neurogenic arthrogryposis multiplex congenita	Has interpretation	Decreased	true	Inferred relationship	Existential restriction modifier	4
Neurogenic arthrogryposis multiplex congenita	Interprets	Range of joint movement	true	Inferred relationship	Existential restriction modifier	4

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Arthrogryposis with renal dysfunction and cholestasis syndrome	Is a	True	Neurogenic arthrogryposis multiplex congenita	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3302194018	Neurogenic arthrogryposis multiplex congenita (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3302195017	Neurogenic arthrogryposis multiplex congenita	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module