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719990003: autosomaal dominante 'limb-girdle'-spierdystrofie type 1G (aandoening)


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
3318734013 Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3318735014 Autosomal dominant limb girdle muscular dystrophy type 1G en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
6699491000146118 LGMD1G nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7880461000146113 autosomaal dominante 'limb-girdle'-spierdystrofie type 1G (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7880471000146119 autosomaal dominante 'limb-girdle'-spierdystrofie type 1G nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7880481000146117 autosomaal dominante 'limb-girdle muscular dystrophy' type 1G nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7880491000146115 autosomaal dominante gordeldystrofie type 1G nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
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 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 1G (disorder) Is a Autosomal dominant muscular dystrophy with limb girdle distribution true Inferred relationship Some
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 3
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) Occurrence Congenital false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) Associated morphology Dystrophy false Inferred relationship Some 3
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) Finding site Skeletal muscle structure true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1G (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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