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230561007: Congenital neuropathy with arthrogryposis multiplex congenita (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2023. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
neuropathie congénitale avec arthrogrypose multiple congénitale	Is a	Congenital polyneuropathy	false	Inferred relationship	Some
neuropathie congénitale avec arthrogrypose multiple congénitale	Finding site	Peripheral nervous system structure	false	Inferred relationship	Some	2
neuropathie congénitale avec arthrogrypose multiple congénitale	Finding site	Nerve structure	false	Inferred relationship	Some	1
neuropathie congénitale avec arthrogrypose multiple congénitale	Occurrence	Congenital	false	Inferred relationship	Some
neuropathie congénitale avec arthrogrypose multiple congénitale	Is a	Neuropathy (disorder)	false	Inferred relationship	Some
neuropathie congénitale avec arthrogrypose multiple congénitale	Is a	Congenital anomaly of the peripheral nervous system	false	Inferred relationship	Some
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	2
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	2
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	2
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	2
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	2
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	2
neuropathie congénitale avec arthrogrypose multiple congénitale	Occurrence	Congenital	false	Inferred relationship	Some	3
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Developmental anomaly	false	Inferred relationship	Some	3
neuropathie congénitale avec arthrogrypose multiple congénitale	Finding site	Peripheral nervous system structure	false	Inferred relationship	Some	3
neuropathie congénitale avec arthrogrypose multiple congénitale	Is a	Congenital anomaly of joint	false	Inferred relationship	Some
neuropathie congénitale avec arthrogrypose multiple congénitale	Occurrence	Congenital	false	Inferred relationship	Some	2
neuropathie congénitale avec arthrogrypose multiple congénitale	Occurrence	Congenital	false	Inferred relationship	Some	4
neuropathie congénitale avec arthrogrypose multiple congénitale	Occurrence	Congenital	false	Inferred relationship	Some	5
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Contracture	false	Inferred relationship	Some	5
neuropathie congénitale avec arthrogrypose multiple congénitale	Finding site	Joint structure	false	Inferred relationship	Some	5
neuropathie congénitale avec arthrogrypose multiple congénitale	Is a	Arthrogryposis	false	Inferred relationship	Some
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Developmental anomaly	false	Inferred relationship	Some	2
neuropathie congénitale avec arthrogrypose multiple congénitale	Finding site	Joint structure	false	Inferred relationship	Some	2
neuropathie congénitale avec arthrogrypose multiple congénitale	Finding site	Nerve structure	false	Inferred relationship	Some	4
neuropathie congénitale avec arthrogrypose multiple congénitale	Associated morphology	Contracture	false	Inferred relationship	Some	2
neuropathie congénitale avec arthrogrypose multiple congénitale	Occurrence	Congenital	false	Inferred relationship	Some	1
neuropathie congénitale avec arthrogrypose multiple congénitale	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	2
neuropathie congénitale avec arthrogrypose multiple congénitale	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	1
neuropathie congénitale avec arthrogrypose multiple congénitale	Interprets	Range of joint movement	false	Inferred relationship	Some	3
neuropathie congénitale avec arthrogrypose multiple congénitale	Has interpretation	Decreased	false	Inferred relationship	Some	3
neuropathie congénitale avec arthrogrypose multiple congénitale	Finding site	Structure of joint region	false	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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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
5739961000172110	neuropathie congénitale avec arthrogrypose multiple congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
4917801000172117	aangeboren neuropathie met arthrogryposis multiplex congenita	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
4917811000172119	congenitale neuropathie met arthrogryposis multiplex congenita	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)