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726615005: Autosomal recessive limb girdle muscular dystrophy type 2Q (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
3450992015 Autosomal recessive limb girdle muscular dystrophy type 2Q (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3450993013 Autosomal recessive limb girdle muscular dystrophy type 2Q en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5403553010 A form of limb-girdle muscular dystrophy characterized by proximal muscle weakness presenting in early childhood (with occasional falls and difficulties in climbing stairs) and a progressive course resulting in loss of ambulation in early adulthood. Muscle atrophy and multiple contractures have also been reported in rare cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403554016 A form of limb-girdle muscular dystrophy characterised by proximal muscle weakness presenting in early childhood (with occasional falls and difficulties in climbing stairs) and a progressive course resulting in loss of ambulation in early adulthood. Muscle atrophy and multiple contractures have also been reported in rare cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3450992015 Autosomal recessive limb girdle muscular dystrophy type 2Q (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3450993013 Autosomal recessive limb girdle muscular dystrophy type 2Q en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3450994019 A form of limb-girdle muscular dystrophy with characteristics of proximal muscle weakness presenting in early childhood (with occasional falls and difficulties in climbing stairs) and a progressive course resulting in loss of ambulation in early adulthood. Muscle atrophy and multiple contractures have also been reported in rare cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403553010 A form of limb-girdle muscular dystrophy characterized by proximal muscle weakness presenting in early childhood (with occasional falls and difficulties in climbing stairs) and a progressive course resulting in loss of ambulation in early adulthood. Muscle atrophy and multiple contractures have also been reported in rare cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403554016 A form of limb-girdle muscular dystrophy characterised by proximal muscle weakness presenting in early childhood (with occasional falls and difficulties in climbing stairs) and a progressive course resulting in loss of ambulation in early adulthood. Muscle atrophy and multiple contractures have also been reported in rare cases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3443601001000119 Plectin-assoziierte Gliedergürtelmuskeldystrophie R17 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
901721000172118 LGMD2Q - limb-girdle muscular dystrophy type 2Q fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
971581000172119 dystrophie musculaire des ceintures autosomique récessive type 2Q fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
901721000172118 LGMD2Q - limb-girdle muscular dystrophy type 2Q fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
971581000172119 dystrophie musculaire des ceintures autosomique récessive type 2Q fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3443601001000119 Plectin-assoziierte Gliedergürtelmuskeldystrophie R17 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 2Q (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 2Q (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2Q (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2Q (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 2Q (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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