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230561007: Congenital neuropathy with arthrogryposis multiplex congenita (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Deformity (finding)\Congenital deformity\Arthrogryposis\Congenital neuropathy with arthrogryposis multiplex congenita
\Deformity (finding)\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Congenital neuropathy with arthrogryposis multiplex congenita

\Finding of movement (finding)\Finding of joint movement\Finding of range of joint movement\Limitation of joint movement\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Congenital neuropathy with arthrogryposis multiplex congenita
\Finding of movement (finding)\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\Disorder of body system\Disorder of nervous system (disorder)\Neuropathy (disorder)\Congenital neuropathy with arthrogryposis multiplex congenita
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital deformity\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\Developmental disorder\Congenital malformation\Congenital deformity\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

2801461000052116 kongenital neuropati med arthrogryphosis multiplex congenita sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital neuropathy with arthrogryposis multiplex congenita	Is a	Congenital polyneuropathy	false	Inferred relationship	Some
Congenital neuropathy with arthrogryposis multiplex congenita	Finding site	Peripheral nervous system structure	false	Inferred relationship	Some	2
Congenital neuropathy with arthrogryposis multiplex congenita	Finding site	Nerve structure	true	Inferred relationship	Some	1
Congenital neuropathy with arthrogryposis multiplex congenita	Occurrence	Congenital	false	Inferred relationship	Some
Congenital neuropathy with arthrogryposis multiplex congenita	Is a	Neuropathy (disorder)	true	Inferred relationship	Some
Congenital neuropathy with arthrogryposis multiplex congenita	Is a	Congenital anomaly of the peripheral nervous system	false	Inferred relationship	Some
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	kongenital anomali	false	Inferred relationship	Some	1
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	kongenital anomali	false	Inferred relationship	Some	2
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	kongenital anomali	false	Inferred relationship	Some	1
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	kongenital anomali	false	Inferred relationship	Some	2
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	kongenital anomali	false	Inferred relationship	Some	1
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	kongenital anomali	false	Inferred relationship	Some	2
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	kongenital anomali	false	Inferred relationship	Some	1
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	kongenital anomali	false	Inferred relationship	Some	2
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	kongenital anomali	false	Inferred relationship	Some	1
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	kongenital anomali	false	Inferred relationship	Some	2
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	kongenital anomali	false	Inferred relationship	Some	1
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	kongenital anomali	false	Inferred relationship	Some	2
Congenital neuropathy with arthrogryposis multiplex congenita	Occurrence	Congenital	false	Inferred relationship	Some	3
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	utvecklingsabnormitet	false	Inferred relationship	Some	3
Congenital neuropathy with arthrogryposis multiplex congenita	Finding site	Peripheral nervous system structure	false	Inferred relationship	Some	3
Congenital neuropathy with arthrogryposis multiplex congenita	Is a	Congenital anomaly of joint	false	Inferred relationship	Some
Congenital neuropathy with arthrogryposis multiplex congenita	Occurrence	Congenital	true	Inferred relationship	Some	2
Congenital neuropathy with arthrogryposis multiplex congenita	Occurrence	Congenital	false	Inferred relationship	Some	4
Congenital neuropathy with arthrogryposis multiplex congenita	Occurrence	Congenital	false	Inferred relationship	Some	5
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	Contracture	false	Inferred relationship	Some	5
Congenital neuropathy with arthrogryposis multiplex congenita	Finding site	Joint structure	false	Inferred relationship	Some	5
Congenital neuropathy with arthrogryposis multiplex congenita	Is a	Arthrogryposis	true	Inferred relationship	Some
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	utvecklingsabnormitet	false	Inferred relationship	Some	2
Congenital neuropathy with arthrogryposis multiplex congenita	Finding site	Joint structure	false	Inferred relationship	Some	2
Congenital neuropathy with arthrogryposis multiplex congenita	Finding site	Nerve structure	false	Inferred relationship	Some	4
Congenital neuropathy with arthrogryposis multiplex congenita	Associated morphology	Contracture	true	Inferred relationship	Some	2
Congenital neuropathy with arthrogryposis multiplex congenita	Occurrence	Congenital	true	Inferred relationship	Some	1
Congenital neuropathy with arthrogryposis multiplex congenita	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	2
Congenital neuropathy with arthrogryposis multiplex congenita	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Congenital neuropathy with arthrogryposis multiplex congenita	Interprets	Range of joint movement	true	Inferred relationship	Some	3
Congenital neuropathy with arthrogryposis multiplex congenita	Has interpretation	Decreased	true	Inferred relationship	Some	3
Congenital neuropathy with arthrogryposis multiplex congenita	Finding site	Structure of joint region	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

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
2801461000052116	kongenital neuropati med arthrogryphosis multiplex congenita	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)