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240104008: Congenital myotonic dystrophy (disorder)


Status: current, Defined. Date: 31-Oct 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
359716010 Congenital myotonic dystrophy en Synonym Active Case insensitive SNOMED CT core
629203015 Congenital myotonic dystrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital myotonic dystrophy Is a Myotonic dystrophy true Inferred relationship Some
Congenital myotonic dystrophy Clinical course Progressive true Inferred relationship Some 2
Congenital myotonic dystrophy Pathological process Pathological developmental process true Inferred relationship Some 1
Congenital myotonic dystrophy Is a Congenital hereditary muscular dystrophy true Inferred relationship Some
Congenital myotonic dystrophy Is a Myotonic disorder false Inferred relationship Some
Congenital myotonic dystrophy Is a Congenital disease false Inferred relationship Some
Congenital myotonic dystrophy Occurrence Congenital false Inferred relationship Some
Congenital myotonic dystrophy Occurrence Congenital true Inferred relationship Some 1
Congenital myotonic dystrophy Finding site Skeletal muscle structure true Inferred relationship Some 1
Congenital myotonic dystrophy Occurrence Congenital false Inferred relationship Some
Congenital myotonic dystrophy Finding site Skeletal muscle structure false Inferred relationship Some
Congenital myotonic dystrophy Finding site Brain structure false Inferred relationship Some
Congenital myotonic dystrophy Associated morphology Dystrophy true Inferred relationship Some 1
Congenital myotonic dystrophy Is a Myopathy false Inferred relationship Some
Congenital myotonic dystrophy Is a Steinert myotonic dystrophy syndrome false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

REPLACED BY association reference set

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