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732929002: Autosomal recessive limb girdle muscular dystrophy type 2S (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3467531016 Autosomal recessive limb girdle muscular dystrophy type 2S (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3467532011 Autosomal recessive limb girdle muscular dystrophy type 2S en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5403639018 A form of limb-girdle muscular dystrophy characterized by childhood-onset of progressive proximal muscle weakness (leading to reduced ambulation) with myalgia and fatigue, in addition to infantile hyperkinetic movements, truncal ataxia, and intellectual disability. Additional manifestations include scoliosis, hip dysplasia, and less commonly, ocular features (e.g. myopia, cataract) and seizures. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403640016 A form of limb-girdle muscular dystrophy characterised by childhood-onset of progressive proximal muscle weakness (leading to reduced ambulation) with myalgia and fatigue, in addition to infantile hyperkinetic movements, truncal ataxia, and intellectual disability. Additional manifestations include scoliosis, hip dysplasia, and less commonly, ocular features (e.g. myopia, cataract) and seizures. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3467531016 Autosomal recessive limb girdle muscular dystrophy type 2S (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3467532011 Autosomal recessive limb girdle muscular dystrophy type 2S en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3467533018 A form of limb-girdle muscular dystrophy with characteristics of childhood-onset progressive proximal muscle weakness (leading to reduced ambulation) with myalgia and fatigue, in addition to infantile hyperkinetic movements, truncal ataxia, and intellectual disability. Additional manifestations include scoliosis, hip dysplasia, and less commonly ocular features (e.g. myopia, cataract) and seizures. There is evidence that this disease is caused by homozygous or compound heterozygous mutation in the TRAPPC11 gene on chromosome 4q35. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403639018 A form of limb-girdle muscular dystrophy characterized by childhood-onset of progressive proximal muscle weakness (leading to reduced ambulation) with myalgia and fatigue, in addition to infantile hyperkinetic movements, truncal ataxia, and intellectual disability. Additional manifestations include scoliosis, hip dysplasia, and less commonly, ocular features (e.g. myopia, cataract) and seizures. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403640016 A form of limb-girdle muscular dystrophy characterised by childhood-onset of progressive proximal muscle weakness (leading to reduced ambulation) with myalgia and fatigue, in addition to infantile hyperkinetic movements, truncal ataxia, and intellectual disability. Additional manifestations include scoliosis, hip dysplasia, and less commonly, ocular features (e.g. myopia, cataract) and seizures. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3415921001000111 TRAPPC11-assoziierte Gliedergürtelmuskeldystrophie R18 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
944861000172113 LGMD2S - limb-girdle muscular dystrophy type 2S fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
949141000172117 dystrophie musculaire des ceintures autosomique récessive type 2S fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
944861000172113 LGMD2S - limb-girdle muscular dystrophy type 2S fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
949141000172117 dystrophie musculaire des ceintures autosomique récessive type 2S fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3415921001000111 TRAPPC11-assoziierte Gliedergürtelmuskeldystrophie R18 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive limb girdle muscular dystrophy type 2S (disorder) Is a Autosomal recessive muscular dystrophy with limb girdle distribution (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive limb girdle muscular dystrophy type 2S (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2S (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2S (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2S (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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