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715340002: Autosomal recessive limb girdle muscular dystrophy type 2D (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3302268016 Alpha-sarcoglycanopathy LGMD2D (limb girdle muscular dystrophy type 2D) en Synonym Active Initial character case insensitive SNOMED CT core
3302279014 Autosomal recessive limb girdle muscular dystrophy type 2D (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3302280012 Autosomal recessive limb girdle muscular dystrophy type 2D en Synonym Active Initial character case insensitive SNOMED CT core
3302281011 Limb girdle muscular dystrophy characterized by limb-girdle weakness and calf pseudohypertrophy. en Definition Active Case sensitive SNOMED CT core
3302282016 Limb girdle muscular dystrophy characterised by limb-girdle weakness and calf pseudohypertrophy. 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 2D Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2D Clinical course Progressive true Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2D Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Some
Autosomal recessive limb girdle muscular dystrophy type 2D Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2D 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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