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399091004: Facioscapulohumeral muscular dystrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1767011017 Facioscapulohumeral muscular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1778554019 Facioscapulohumeral muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786683010 FSH - Facioscapulohumeral muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1786684016 Landouzy-Déjérine muscular dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786685015 Landouzy-Dejerine muscular dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786686019 FSHD - Facioscapulohumeral muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1786687011 FMD - Facioscapulohumeral muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1786688018 Fascioscapulohumeral muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
423131000172114 dystrophie musculaire facioscapulohumérale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
2235201000172111 dystrophie musculaire facio-scapulo-humérale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
443641000172114 facioscapulohumerale spierdystrofie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Facioscapulohumeral muscular dystrophy (disorder) Is a Autosomal dominant muscular dystrophy not predominantly limb girdle true Inferred relationship Some
Facioscapulohumeral muscular dystrophy (disorder) Occurrence Congenital false Inferred relationship Some
Facioscapulohumeral muscular dystrophy (disorder) Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 1
Facioscapulohumeral muscular dystrophy (disorder) Associated morphology Congenital anomaly false Inferred relationship Some 2
Facioscapulohumeral muscular dystrophy (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Facioscapulohumeral muscular dystrophy (disorder) Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 2
Facioscapulohumeral muscular dystrophy (disorder) Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 1
Facioscapulohumeral muscular dystrophy (disorder) Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 2
Facioscapulohumeral muscular dystrophy (disorder) Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 1
Facioscapulohumeral muscular dystrophy (disorder) Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 2
Facioscapulohumeral muscular dystrophy (disorder) Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 1
Facioscapulohumeral muscular dystrophy (disorder) Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 2
Facioscapulohumeral muscular dystrophy (disorder) Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 1
Facioscapulohumeral muscular dystrophy (disorder) Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 2
Facioscapulohumeral muscular dystrophy (disorder) Finding site Skeletal muscle structure (body structure) true Inferred relationship Some 1
Facioscapulohumeral muscular dystrophy (disorder) Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 2
Facioscapulohumeral muscular dystrophy (disorder) Occurrence Congenital false Inferred relationship Some 3
Facioscapulohumeral muscular dystrophy (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 3
Facioscapulohumeral muscular dystrophy (disorder) Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 3
Facioscapulohumeral muscular dystrophy (disorder) Occurrence Congenital false Inferred relationship Some 2
Facioscapulohumeral muscular dystrophy (disorder) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
Facioscapulohumeral muscular dystrophy (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 2
Facioscapulohumeral muscular dystrophy (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Facioscapulohumeral muscular dystrophy (disorder) Occurrence Congenital true Inferred relationship Some 1
Facioscapulohumeral muscular dystrophy (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Belgian GP subset (foundation metadata concept)

Belgian subset for medical problems in patient health records

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