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719990003: Autosomal dominant limb girdle muscular dystrophy type 1G (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3318734013 Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3318735014 Autosomal dominant limb girdle muscular dystrophy type 1G en Synonym Active Initial character case insensitive SNOMED CT core
3318736010 A mild form of limb girdle muscular dystrophy that has characteristics of limb-girdle weakness, marked proximal amyotrophy and abolished myotatic reflexes, associated with progressive fingers and toes flexion limitation. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant limb girdle muscular dystrophy type 1G Finding site Skeletal muscle structure true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1G Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1G Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1G Clinical course Progressive true Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1G Is a Autosomal dominant muscular dystrophy with limb girdle distribution true Inferred relationship Some
Autosomal dominant limb girdle muscular dystrophy type 1G Finding site Skeletal muscle structure false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1G Finding site Skeletal muscle structure false Inferred relationship Some 3
Autosomal dominant limb girdle muscular dystrophy type 1G Associated morphology Developmental abnormality false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1G Occurrence Congenital false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1G Associated morphology Dystrophy false Inferred relationship Some 3

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

Description inactivation indicator reference set

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