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720522001: Autosomal recessive limb girdle muscular dystrophy type 2G (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3321124019 Autosomal recessive limb girdle muscular dystrophy type 2G (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3321125018 Autosomal recessive limb girdle muscular dystrophy type 2G en Synonym Active Initial character case insensitive SNOMED CT core
3321126017 Limb girdle muscular dystrophy due to telethonin deficiency en Synonym Active Case insensitive SNOMED CT core
3321127014 A mild form of limb-girdle muscular dystrophy with characteristics of muscle weakness in the four limbs, mild scapular winging, severe atrophy of the quadriceps and anterior tibialis muscles, calf hypertrophy and lack of respiratory and cardiac involvement. 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 2G Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2G Clinical course Progressive true Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2G Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Some
Autosomal recessive limb girdle muscular dystrophy type 2G Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2G 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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