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719987009: Autosomal dominant limb girdle muscular dystrophy type 1D (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3318725015 Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3318726019 Autosomal dominant limb girdle muscular dystrophy type 1D en Synonym Active Initial character case insensitive SNOMED CT core
3318727011 A limb girdle muscular dystrophy with characteristics of muscular weakness, primarily affecting the pelvic and shoulder girdles with no bulbar weakness or dysarthria. 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 1D Finding site Skeletal muscle structure true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1D Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1D Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1D Clinical course Progressive true Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1D Is a Autosomal dominant muscular dystrophy with limb girdle distribution true Inferred relationship Some
Autosomal dominant limb girdle muscular dystrophy type 1D Finding site Skeletal muscle structure false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1D Finding site Skeletal muscle structure false Inferred relationship Some 3
Autosomal dominant limb girdle muscular dystrophy type 1D Associated morphology Developmental abnormality false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1D Occurrence Congenital false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1D 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

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