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718179003: Autosomal recessive limb girdle muscular dystrophy type 2B (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3311392019 Autosomal recessive limb girdle muscular dystrophy type 2B (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3311393012 Autosomal recessive limb girdle muscular dystrophy type 2B en Synonym Active Initial character case insensitive SNOMED CT core
3311394018 Limb girdle muscular dystrophy due to dysferlin deficiency en Synonym Active Case insensitive SNOMED CT core
3311395017 Autosomal recessive limb-girdle muscular dystrophy type 2B (LGMD2B) is a limb-girdle muscular dystrophy with characteristics of limb-girdle weakness and atrophy mostly in the shoulder pelvic girdle. Cardiac and respiratory muscles are not involved. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive limb girdle muscular dystrophy type 2B Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2B Clinical course Progressive true Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2B Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Some
Autosomal recessive limb girdle muscular dystrophy type 2B Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2B Finding site Skeletal muscle structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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