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240104008: Congenital myotonic dystrophy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Oct 2021. Module: SNOMED CT core module

Descriptions:

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


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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