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718176005: Autosomal recessive limb girdle muscular dystrophy type 2C (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
3311380019 Autosomal recessive limb girdle muscular dystrophy type 2C (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311381015 Autosomal recessive limb girdle muscular dystrophy type 2C en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311382010 Limb girdle muscular dystrophy due to gamma-sarcoglycan deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401691011 A subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a childhood onset of progressive shoulder and pelvic girdle muscle weakness and atrophy frequently associated with calf hypertrophy, diaphragmatic weakness, and/or variable cardiac abnormalities. Mild to moderate elevated serum creatine kinase levels and positive Gowers sign are reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401692016 A subtype of autosomal recessive limb-girdle muscular dystrophy characterised by a childhood onset of progressive shoulder and pelvic girdle muscle weakness and atrophy frequently associated with calf hypertrophy, diaphragmatic weakness, and/or variable cardiac abnormalities. Mild to moderate elevated serum creatine kinase levels and positive Gowers sign are reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3311380019 Autosomal recessive limb girdle muscular dystrophy type 2C (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311381015 Autosomal recessive limb girdle muscular dystrophy type 2C en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311382010 Limb girdle muscular dystrophy due to gamma-sarcoglycan deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311382010 Limb girdle muscular dystrophy due to gamma-sarcoglycan deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311384011 Autosomal recessive limb girdle muscular dystrophy type 2C (LGMD2C) is a limb girdle muscular dystrophy with manifestations of limb-girdle weakness, calf hypertrophy, diaphragmatic weakness and variable cardiac abnormalities. Ambulation may be lost by the age 12. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401691011 A subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a childhood onset of progressive shoulder and pelvic girdle muscle weakness and atrophy frequently associated with calf hypertrophy, diaphragmatic weakness, and/or variable cardiac abnormalities. Mild to moderate elevated serum creatine kinase levels and positive Gowers sign are reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401692016 A subtype of autosomal recessive limb-girdle muscular dystrophy characterised by a childhood onset of progressive shoulder and pelvic girdle muscle weakness and atrophy frequently associated with calf hypertrophy, diaphragmatic weakness, and/or variable cardiac abnormalities. Mild to moderate elevated serum creatine kinase levels and positive Gowers sign are reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3391371001000117 Gamma-Sarkoglykan-assoziierte Gliedergürtelmuskeldystrophie R5 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
901541000172115 dystrophie musculaire des ceintures autosomique récessive type 2C fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
930671000172112 dystrophie musculaire des ceintures par déficit en gamma-sarcoglycane fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
901541000172115 dystrophie musculaire des ceintures autosomique récessive type 2C fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
930671000172112 dystrophie musculaire des ceintures par déficit en gamma-sarcoglycane fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3391371001000117 Gamma-Sarkoglykan-assoziierte Gliedergürtelmuskeldystrophie R5 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 2C (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 2C (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2C (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2C (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 2C (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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