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715316005: Neurogenic arthrogryposis multiplex congenita (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3302194018 Neurogenic arthrogryposis multiplex congenita (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302195017 Neurogenic arthrogryposis multiplex congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5400817019 A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400818012 A form of arthrogryposis multiplex congenita characterised by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3302194018 Neurogenic arthrogryposis multiplex congenita (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3302194018 Neurogenic arthrogryposis multiplex congenita (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302195017 Neurogenic arthrogryposis multiplex congenita en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3302195017 Neurogenic arthrogryposis multiplex congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302201013 A form of arthrogryposis multiplex congenital characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscular atrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3302202018 A form of arthrogryposis multiplex congenital characterised by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscular atrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400817019 A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400818012 A form of arthrogryposis multiplex congenita characterised by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3435701001000111 Arthrogryposis multiplex congenita, neurogener Typ de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
956421000172114 arthrogrypose congénitale multiple neurogénique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
956421000172114 arthrogrypose congénitale multiple neurogénique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3435701001000111 Arthrogryposis multiplex congenita, neurogener Typ de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Due to Denervation atrophy of muscle true Inferred relationship Existential restriction modifier (core metadata concept) 3
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Is a Arthropathy associated with another disorder false Inferred relationship Existential restriction modifier (core metadata concept)
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Is a Arthrogryposis false Inferred relationship Existential restriction modifier (core metadata concept)
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Associated morphology Contracture true Inferred relationship Existential restriction modifier (core metadata concept) 2
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Finding site Joint structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Associated morphology Contracture true Inferred relationship Existential restriction modifier (core metadata concept) 1
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Interprets Range of joint movement false Inferred relationship Existential restriction modifier (core metadata concept) 2
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Finding site Structure of joint region true Inferred relationship Existential restriction modifier (core metadata concept) 1
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Has interpretation Absent false Inferred relationship Existential restriction modifier (core metadata concept) 2
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Is a Joint movement absent false Inferred relationship Existential restriction modifier (core metadata concept)
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Is a Inherited arthrogryposis true Inferred relationship Existential restriction modifier (core metadata concept)
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Has interpretation Decreased true Inferred relationship Existential restriction modifier (core metadata concept) 4
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Interprets Range of joint movement true Inferred relationship Existential restriction modifier (core metadata concept) 4
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Is a A group of disorders with characteristics of congenital limb contractures manifesting as limitation of movement of multiple limb joints at birth that is usually non-progressive and may include muscle weakness and fibrosis. This disorder is always associated with decreased intrauterine fetal movement, which leads secondarily to the contractures. true Inferred relationship Existential restriction modifier (core metadata concept)
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Is a Polyarthropathy associated with another disorder true Inferred relationship Existential restriction modifier (core metadata concept)
A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Finding site Joint structure of multiple body sites (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Arthrogryposis with renal dysfunction and cholestasis syndrome (disorder) Is a True A form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy. Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Description inactivation indicator reference set

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