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1177122009: Myotonic dystrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Oct 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4643487015 Myotonic dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4643488013 DM - dystrophia myotonica en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4643489017 Myotonia dystrophica en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4643490014 Myotonic dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4643491013 Dystrophia myotonica en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4643487015 Myotonic dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4643488013 DM - dystrophia myotonica en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4643489017 Myotonia dystrophica en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4643490014 Myotonic dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4643491013 Dystrophia myotonica en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myotonic dystrophy (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Myotonic dystrophy (disorder) Is a Hereditary progressive muscular dystrophy true Inferred relationship Existential restriction modifier (core metadata concept)
Myotonic dystrophy (disorder) Is a Myotonic disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Myotonic dystrophy (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2
Myotonic dystrophy (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Myotonic dystrophy (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Myotonic dystrophy (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Steinert myotonic dystrophy syndrome Is a True Myotonic dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare myotonic dystrophy of juvenile or adult-onset characterised by mild and fluctuating myotonia, muscle weakness, and rarely cardiac conduction disorders. Is a True Myotonic dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cardiomyopathy in myotonic dystrophy Associated with True Myotonic dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital myotonic dystrophy Is a True Myotonic dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Dilated cardiomyopathy secondary to myotonic dystrophy Due to True Myotonic dystrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 2

This concept is not in any reference sets

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