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387732009: Becker-spierdystrofie (aandoening)


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

Descriptions:

Id Description Lang Type Status Case? Module
1461910018 Becker muscular dystrophy (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1481810012 Becker muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1492251019 Becker's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1492252014 BMD - Becker muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1785296012 Becker's muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1785297015 Benign Duchenne muscular dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
11591000146111 spierdystrofie van Becker nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
728821000146113 BMD nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13015931000146114 Becker-spierdystrofie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13015941000146118 Becker-spierdystrofie (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13672441000146117 Becker muscular dystrophy nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7577151000146112 Dit is een zeldzame spierziekte die alleen bij mannen voorkomt. nl Definition Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Becker muscular dystrophy (disorder) Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 2
Becker muscular dystrophy (disorder) Is a X-linked muscular dystrophy with abnormal dystrophin true Inferred relationship Some
Becker muscular dystrophy (disorder) Occurrence Congenital false Inferred relationship Some
Becker muscular dystrophy (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 1
Becker muscular dystrophy (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Becker muscular dystrophy (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 2
Becker muscular dystrophy (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 1
Becker muscular dystrophy (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 2
Becker muscular dystrophy (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 1
Becker muscular dystrophy (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 2
Becker muscular dystrophy (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 1
Becker muscular dystrophy (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 2
Becker muscular dystrophy (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 1
Becker muscular dystrophy (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 2
Becker muscular dystrophy (disorder) Finding site Skeletal muscle structure true Inferred relationship Some 1
Becker muscular dystrophy (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 2
Becker muscular dystrophy (disorder) Occurrence Congenital false Inferred relationship Some 3
Becker muscular dystrophy (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3
Becker muscular dystrophy (disorder) Finding site Skeletal muscle structure false Inferred relationship Some 3
Becker muscular dystrophy (disorder) Occurrence Congenital false Inferred relationship Some 2
Becker muscular dystrophy (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 2
Becker muscular dystrophy (disorder) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
Becker muscular dystrophy (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Becker muscular dystrophy (disorder) Occurrence Congenital true Inferred relationship Some 1
Becker muscular dystrophy (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Cardiomyopathy associated with Becker muscular dystrophy (disorder) Associated with True Becker muscular dystrophy (disorder) Inferred relationship Some 1

Reference Sets

Dutch rare neuromuscular disorders simple reference set (foundation metadata concept)

Dutch pathology simple reference set (foundation metadata concept)

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