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718177001: Autosomal recessive limb girdle muscular dystrophy type 2F (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
3311383017 Autosomal recessive limb girdle muscular dystrophy type 2F (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311385012 Autosomal recessive limb girdle muscular dystrophy type 2F en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311386013 Limb girdle muscular dystrophy due to delta-sarcoglycan deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401693014 A subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a variable age of onset of progressive weakness and wasting of the proximal skeletal muscles of the shoulder and pelvic girdles, frequently associated with progressive respiratory muscle impairment and cardiomyopathy. Calf hypertrophy, muscle cramps and elevated serum creatine kinase levels are also observed. Neuro-psychomotor development is usually normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401694015 A subtype of autosomal recessive limb-girdle muscular dystrophy characterised by a variable age of onset of progressive weakness and wasting of the proximal skeletal muscles of the shoulder and pelvic girdles, frequently associated with progressive respiratory muscle impairment and cardiomyopathy. Calf hypertrophy, muscle cramps and elevated serum creatine kinase levels are also observed. Neuro-psychomotor development is usually normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3311383017 Autosomal recessive limb girdle muscular dystrophy type 2F (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311385012 Autosomal recessive limb girdle muscular dystrophy type 2F en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311386013 Limb girdle muscular dystrophy due to delta-sarcoglycan deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311386013 Limb girdle muscular dystrophy due to delta-sarcoglycan deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311387016 Autosomal recessive limb-girdle muscular dystrophy type 2F (LGMD2F) is a limb-girdle muscular dystrophy with manifestations of limb-girdle weakness, cardiomyopathy and respiratory impairment. LGMD2F is caused by a deficit of a sarcoglycan protein and therefore belongs to a group of disorders named sarcoglycanopathy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401693014 A subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a variable age of onset of progressive weakness and wasting of the proximal skeletal muscles of the shoulder and pelvic girdles, frequently associated with progressive respiratory muscle impairment and cardiomyopathy. Calf hypertrophy, muscle cramps and elevated serum creatine kinase levels are also observed. Neuro-psychomotor development is usually normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401694015 A subtype of autosomal recessive limb-girdle muscular dystrophy characterised by a variable age of onset of progressive weakness and wasting of the proximal skeletal muscles of the shoulder and pelvic girdles, frequently associated with progressive respiratory muscle impairment and cardiomyopathy. Calf hypertrophy, muscle cramps and elevated serum creatine kinase levels are also observed. Neuro-psychomotor development is usually normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3387211001000113 Delta-Sarkoglykan-assoziierte Gliedergürtelmuskeldystrophie R6 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
922361000172112 delta-sarcoglycanopathie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
962191000172114 dystrophie musculaire des ceintures autosomique récessive type 2F fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
922361000172112 delta-sarcoglycanopathie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
962191000172114 dystrophie musculaire des ceintures autosomique récessive type 2F fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3387211001000113 Delta-Sarkoglykan-assoziierte Gliedergürtelmuskeldystrophie R6 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 2F 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 2F Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2F Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2F 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 2F 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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