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76670001: Duchenne-spierdystrofie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
127307018 Duchenne muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
127308011 Pseudohypertrophic muscular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
503329018 DMD - Duchenne muscular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
817415014 Duchenne muscular dystrophy (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
12211000146114 ziekte van Duchenne nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
56761000146113 musculaire dystrofie van Duchenne nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
729161000146118 DMD nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13015951000146115 Duchenne-spierdystrofie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13015961000146117 Duchenne-spierdystrofie (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13672541000146118 Duchenne muscular dystrophy nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7680601000146119 Duchenne-spierdystrofie (DMD) is een zeldzame, erfelijke, snel verergerende spierziekte die alleen bij jongens 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
Duchenne muscular dystrophy Is a X-linked muscular dystrophy with abnormal dystrophin true Inferred relationship Some
Duchenne muscular dystrophy Associated morphology Pseudohypertrophic dystrophy true Inferred relationship Some 1
Duchenne muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Some 2
Duchenne muscular dystrophy Occurrence Congenital false Inferred relationship Some
Duchenne muscular dystrophy Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 2
Duchenne muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Some 1
Duchenne muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Some 1
Duchenne muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Some 2
Duchenne muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Some 2
Duchenne muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Some 1
Duchenne muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Some 2
Duchenne muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Some 1
Duchenne muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Some 2
Duchenne muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Some 1
Duchenne muscular dystrophy Finding site Skeletal muscle structure true Inferred relationship Some 1
Duchenne muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Some 2
Duchenne muscular dystrophy Occurrence Congenital false Inferred relationship Some 3
Duchenne muscular dystrophy Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3
Duchenne muscular dystrophy Finding site Skeletal muscle structure false Inferred relationship Some 3
Duchenne muscular dystrophy Occurrence Congenital false Inferred relationship Some 2
Duchenne muscular dystrophy Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Duchenne muscular dystrophy Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 2
Duchenne muscular dystrophy Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
Duchenne muscular dystrophy Associated morphology Dystrophy false Inferred relationship Some 2
Duchenne muscular dystrophy Clinical course Progressive (qualifier value) true Inferred relationship Some 3
Duchenne muscular dystrophy Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Cardiomyopathy in Duchenne muscular dystrophy Associated with True Duchenne muscular dystrophy Inferred relationship Some 2

Reference Sets

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

Dutch pathology simple reference set (foundation metadata concept)

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