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1366415002: Childhood-onset Steinert myotonic dystrophy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jun 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5459574012 Childhood-onset Steinert disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5459575013 Childhood-onset myotonic dystrophy type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5459576014 Childhood-onset Steinert myotonic dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5459577017 Childhood-onset Steinert myotonic dystrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Childhood-onset Steinert myotonic dystrophy Is a Steinert myotonic dystrophy syndrome true Inferred relationship Some
Childhood-onset Steinert myotonic dystrophy Clinical course Progressive (qualifier value) true Inferred relationship Some 2
Childhood-onset Steinert myotonic dystrophy Occurrence Childhood true Inferred relationship Some 1
Childhood-onset Steinert myotonic dystrophy Finding site Skeletal muscle structure true Inferred relationship Some 1
Childhood-onset Steinert myotonic dystrophy Associated morphology Dystrophy true Inferred relationship Some 1
Childhood-onset Steinert myotonic dystrophy Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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