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726614009: Autosomal recessive limb girdle muscular dystrophy type 2P (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
3450985013 Autosomal recessive limb girdle muscular dystrophy type 2P (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3450986014 Autosomal recessive limb girdle muscular dystrophy type 2P en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5403551012 A form of limb-girdle muscular dystrophy characterized by slowly progressive, mainly proximal, muscle weakness presenting in early childhood (with difficulties walking and climbing stairs) and mild to severe intellectual disability. Additional manifestations reported include microcephaly, mild increase in thigh or calf muscles, and contractures of the ankles. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403552017 A form of limb-girdle muscular dystrophy characterised by slowly progressive, mainly proximal, muscle weakness presenting in early childhood (with difficulties walking and climbing stairs) and mild to severe intellectual disability. Additional manifestations reported include microcephaly, mild increase in thigh or calf muscles, and contractures of the ankles. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3450985013 Autosomal recessive limb girdle muscular dystrophy type 2P (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3450986014 Autosomal recessive limb girdle muscular dystrophy type 2P en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3450987017 A form of limb-girdle muscular dystrophy with characteristics of slowly-progressive mainly proximal muscle weakness presenting in early childhood (with difficulties walking and climbing stairs) and mild to severe intellectual disability. Additional manifestations reported include microcephaly, mild increase in thigh or calf muscles and contractures of the ankles. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403551012 A form of limb-girdle muscular dystrophy characterized by slowly progressive, mainly proximal, muscle weakness presenting in early childhood (with difficulties walking and climbing stairs) and mild to severe intellectual disability. Additional manifestations reported include microcephaly, mild increase in thigh or calf muscles, and contractures of the ankles. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403552017 A form of limb-girdle muscular dystrophy characterised by slowly progressive, mainly proximal, muscle weakness presenting in early childhood (with difficulties walking and climbing stairs) and mild to severe intellectual disability. Additional manifestations reported include microcephaly, mild increase in thigh or calf muscles, and contractures of the ankles. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3388071001000111 Alpha-Dystroglycan-assoziierte Gliedergürtelmuskeldystrophie R16 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
882621000172112 LGMD2P - limb-girdle muscular dystrophy type 2P fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
924691000172116 dystrophie musculaire des ceintures autosomique récessive type 2P fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
882621000172112 LGMD2P - limb-girdle muscular dystrophy type 2P fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
924691000172116 dystrophie musculaire des ceintures autosomique récessive type 2P fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3388071001000111 Alpha-Dystroglycan-assoziierte Gliedergürtelmuskeldystrophie R16 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 2P (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 2P (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2P (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive limb girdle muscular dystrophy type 2P (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 2P (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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