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719987009: dystrophie musculaire des ceintures autosomique dominante type 1D (trouble)


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
3318725015 Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3318726019 Autosomal dominant limb girdle muscular dystrophy type 1D en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
755141000241119 dystrophie musculaire des ceintures autosomique dominante type 1D (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
877301000172116 dystrophie musculaire des ceintures autosomique dominante type 1D fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
884321000172114 LGMD1D - limb-girdle muscular dystrophy type 1D fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
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 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 1D (disorder) localisation d'une constatation (attribut) structure de muscle squelettique true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) morphologie associée (attribut) Dystrophy (morphologic abnormality) true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) évolution clinique (attribut) progressif true Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) est un(e) (attribut) Autosomal dominant muscular dystrophy with limb girdle distribution true Inferred relationship Some
Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some 3
Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) survenue (attribut) congénital false Inferred relationship Some 2
Autosomal dominant limb girdle muscular dystrophy type 1D (disorder) morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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