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718176005: Autosomal recessive limb girdle muscular dystrophy type 2C (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3311380019 Autosomal recessive limb girdle muscular dystrophy type 2C (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3311381015 Autosomal recessive limb girdle muscular dystrophy type 2C en Synonym Active Initial character case insensitive SNOMED CT core
3311382010 Limb girdle muscular dystrophy due to gamma-sarcoglycan deficiency en Synonym Active Case insensitive SNOMED CT core
3311384011 Autosomal recessive limb girdle muscular dystrophy type 2C (LGMD2C) is a limb girdle muscular dystrophy with manifestations of limb-girdle weakness, calf hypertrophy, diaphragmatic weakness and variable cardiac abnormalities. Ambulation may be lost by the age 12. 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 2C Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2C Clinical course Progressive true Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2C Is a Autosomal recessive muscular dystrophy with limb girdle distribution true Inferred relationship Some
Autosomal recessive limb girdle muscular dystrophy type 2C Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2C 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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