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719985001: Autosomal dominant limb girdle muscular dystrophy type 1A (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3318715013 Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3318716014 Autosomal dominant limb girdle muscular dystrophy type 1A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3318717017 Limb girdle muscular dystrophy due to myotilin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3318719019 Limb-girdle muscular dystrophy 1A myotilin myopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3318718010 A limb girdle muscular dystrophy caused by myotilin deficiency with characteristics of limb-girdle weakness in combination with dysarthria. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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