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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
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
129378019 Dystrophia myotonica en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
129378019 Dystrophia myotonica en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
818843014 Steinert myotonic dystrophy syndrome (disorder) en Fully specified name Active Only initial character case insensitive (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
1234184014 Myotonic dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1234184014 Myotonic dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1234185010 DM - Dystrophia myotonica en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1234185010 DM - Dystrophia myotonica en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1234186011 Myotonia dystrophica en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1234186011 Myotonia dystrophica en Synonym (core metadata concept) Active Entire term case insensitive (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
958661000195110 sindrome della distrofia miotonica di Steinert it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3437121001000110 Myotone Dystrophie Steinert de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
120721000172118 dystrophie myotonique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
310871000172112 dystrophie myotonique de Steinert fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
120721000172118 dystrophie myotonique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
310871000172112 dystrophie myotonique de Steinert fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
958661000195110 sindrome della distrofia miotonica di Steinert it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3437121001000110 Myotone Dystrophie Steinert de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


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 Existential restriction modifier (core metadata concept)
Steinert myotonic dystrophy syndrome Is a Congenital anomaly of skeletal muscle (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Steinert myotonic dystrophy syndrome Is a Myotonic disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Steinert myotonic dystrophy syndrome Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Steinert myotonic dystrophy syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Steinert myotonic dystrophy syndrome Associated morphology Dystrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Steinert myotonic dystrophy syndrome Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Steinert myotonic dystrophy syndrome Is a Congenital anomaly of skeletal muscle (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Steinert myotonic dystrophy syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Steinert myotonic dystrophy syndrome Is a Muscular dystrophy false Inferred relationship Existential restriction modifier (core metadata concept)
Steinert myotonic dystrophy syndrome Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Steinert myotonic dystrophy syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Steinert myotonic dystrophy syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Steinert myotonic dystrophy syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Steinert myotonic dystrophy syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Steinert myotonic dystrophy syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Steinert myotonic dystrophy syndrome Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2
Steinert myotonic dystrophy syndrome Is a Hereditary progressive muscular dystrophy false Inferred relationship Existential restriction modifier (core metadata concept)
Steinert myotonic dystrophy syndrome Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Steinert myotonic dystrophy syndrome Is a Myotonic dystrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital myotonic dystrophy Is a False Steinert myotonic dystrophy syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Dilated cardiomyopathy secondary to myotonic dystrophy Associated with False Steinert myotonic dystrophy syndrome Inferred relationship Existential restriction modifier (core metadata concept) 2
Cardiomyopathy in myotonic dystrophy Associated with False Steinert myotonic dystrophy syndrome Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of Steinert myotonic dystrophy (situation) Associated finding True Steinert myotonic dystrophy syndrome Inferred relationship Existential restriction modifier (core metadata concept) 1
Dilated cardiomyopathy secondary to myotonic dystrophy Due to False Steinert myotonic dystrophy syndrome Inferred relationship Existential restriction modifier (core metadata concept) 2

This concept is not in any reference sets

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