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77956009: Steinert myotonic dystrophy syndrome (disorder)


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
129376015 Steinert myotonic dystrophy syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
129377012 Steinert syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
818843014 Steinert myotonic dystrophy syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
4643494017 Myotonic dystrophy type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4643495016 Steinert disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
120721000172118 dystrophie myotonique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
310871000172112 dystrophie myotonique de Steinert fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
2235531000172115 dystrophie musculaire myotonique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
2235541000172110 maladie de Steinert fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
487381000172110 myotone dystrofie type 1 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
531281000172110 ziekte van Steinert nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
2235521000172118 myotone 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
Steinert myotonic dystrophy syndrome Is a Multiple malformation syndrome with unusual brain and/or neuromuscular findings false Inferred relationship Some
Steinert myotonic dystrophy syndrome Is a Congenital anomaly of skeletal muscle false Inferred relationship Some
Steinert myotonic dystrophy syndrome Is a Myotonic disorder false Inferred relationship Some
Steinert myotonic dystrophy syndrome Finding site Brain structure false Inferred relationship Some 2
Steinert myotonic dystrophy syndrome Occurrence Congenital false Inferred relationship Some
Steinert myotonic dystrophy syndrome Associated morphology Dystrophy false Inferred relationship Some 1
Steinert myotonic dystrophy syndrome Finding site Skeletal muscle structure (body structure) false Inferred relationship Some 1
Steinert myotonic dystrophy syndrome Is a Congenital anomaly of skeletal muscle false Inferred relationship Some
Steinert myotonic dystrophy syndrome Associated morphology Congenital malformation false Inferred relationship Some
Steinert myotonic dystrophy syndrome Is a Muscular dystrophy false Inferred relationship Some
Steinert myotonic dystrophy syndrome Finding site Skeletal muscle structure (body structure) true Inferred relationship Some 1
Steinert myotonic dystrophy syndrome Associated morphology Dystrophy true Inferred relationship Some 1
Steinert myotonic dystrophy syndrome Occurrence Congenital false Inferred relationship Some 2
Steinert myotonic dystrophy syndrome Associated morphology Developmental anomaly false Inferred relationship Some 2
Steinert myotonic dystrophy syndrome Occurrence Congenital false Inferred relationship Some 1
Steinert myotonic dystrophy syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Steinert myotonic dystrophy syndrome Clinical course Progressive (qualifier value) true Inferred relationship Some 2
Steinert myotonic dystrophy syndrome Is a Hereditary progressive muscular dystrophy false Inferred relationship Some
Steinert myotonic dystrophy syndrome Is a Autosomal dominant hereditary disorder false Inferred relationship Some
Steinert myotonic dystrophy syndrome Is a Myotonic dystrophy (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital myotonic dystrophy Is a False Steinert myotonic dystrophy syndrome Inferred relationship Some
Dilated cardiomyopathy due to myotonic dystrophy (disorder) Associated with False Steinert myotonic dystrophy syndrome Inferred relationship Some 2
Cardiomyopathy in myotonic dystrophy Associated with False Steinert myotonic dystrophy syndrome Inferred relationship Some 1
Family history of Steinert myotonic dystrophy (situation) Associated finding True Steinert myotonic dystrophy syndrome Inferred relationship Some 1
Dilated cardiomyopathy due to myotonic dystrophy (disorder) Due to False Steinert myotonic dystrophy syndrome Inferred relationship Some 2

Reference Sets

Belgian GP subset (foundation metadata concept)

Belgian subset for medical problems in patient health records

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