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1142324004: Atrophy of peroneal muscle (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4537452016 Atrophy of peroneal muscle (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4537453014 Atrophy of peroneal muscle en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Atrophy of peroneal muscle (disorder) Is a Atrophy of muscle of lower leg (disorder) true Inferred relationship Some
Atrophy of peroneal muscle (disorder) Finding site Peroneal muscle structure true Inferred relationship Some 1
Atrophy of peroneal muscle (disorder) Associated morphology Atrophy true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
A rare, genetic, neuromuscular disease characterized by adult-onset muscle weakness and atrophy in a scapuloperoneal distribution, mild involvement of the facial muscles, dysphagia, and gynecomastia. Elevated serum CK levels and mixed myopathic and neurogenic abnormalities are associated clinical findings. Is a True Atrophy of peroneal muscle (disorder) Inferred relationship Some

This concept is not in any reference sets

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