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725042001: Autosomal recessive limb girdle muscular dystrophy type 2J (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
3437354018 Autosomal recessive limb girdle muscular dystrophy type 2J (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3437355017 Autosomal recessive limb girdle muscular dystrophy type 2J en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3437356016 Limb-girdle muscular dystrophy 2J titin gene mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5403368010 A form of limb-girdle muscular dystrophy that usually has a childhood onset (but can range from the first to third decade of life) of severe progressive proximal weakness, eventually involving the distal muscles. Some patients may remain ambulatory but most are wheelchair dependant 20 years after onset. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3437354018 Autosomal recessive limb girdle muscular dystrophy type 2J (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3437355017 Autosomal recessive limb girdle muscular dystrophy type 2J en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3437356016 Limb-girdle muscular dystrophy 2J titin gene mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3437357013 A form of limb-girdle muscular dystrophy that usually has a childhood onset (but can range from the first to third decade of life) of severe progressive proximal weakness, eventually involving the distal muscles. Some patients may remain ambulatory but most are wheelchair dependant 20 years after onset. Caused by homozygous mutation in the titin gene (TTN). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403368010 A form of limb-girdle muscular dystrophy that usually has a childhood onset (but can range from the first to third decade of life) of severe progressive proximal weakness, eventually involving the distal muscles. Some patients may remain ambulatory but most are wheelchair dependant 20 years after onset. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3412681001000113 Titin-assoziierte Gliedergürtelmuskeldystrophie R10 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
877601000172112 dystrophie musculaire des ceintures autosomique récessive type 2J fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
878541000172114 LGMD2J - limb-girdle muscular dystrophy type 2J fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
877601000172112 dystrophie musculaire des ceintures autosomique récessive type 2J fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
878541000172114 LGMD2J - limb-girdle muscular dystrophy type 2J fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3412681001000113 Titin-assoziierte Gliedergürtelmuskeldystrophie R10 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 2J (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 2J (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2J (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2J (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 2J (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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