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1119438000: Atrophy of muscle of shoulder (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4361991011 Atrophy of muscle of shoulder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4361992016 Atrophy of muscle of shoulder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4361993014 Amyotrophy of muscle of shoulder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Atrophy of muscle of shoulder (disorder) Is a Atrophy of muscle of upper limb (disorder) true Inferred relationship Some
Atrophy of muscle of shoulder (disorder) Is a Disorder of shoulder region (disorder) true Inferred relationship Some
Atrophy of muscle of shoulder (disorder) Finding site Structure of skeletal muscle of shoulder true Inferred relationship Some 1
Atrophy of muscle of shoulder (disorder) Associated morphology Atrophy true Inferred relationship Some 1
Atrophy of muscle of shoulder (disorder) Is a Atrophy of proximal muscle true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Atrophy of latissimus dorsi muscle (disorder) Is a True Atrophy of muscle of shoulder (disorder) Inferred relationship Some
Atrophy of deltoid muscle (disorder) Is a True Atrophy of muscle of shoulder (disorder) Inferred relationship Some
Atrophy of muscle of left shoulder Is a True Atrophy of muscle of shoulder (disorder) Inferred relationship Some
Atrophy of muscle of right shoulder (disorder) Is a True Atrophy of muscle of shoulder (disorder) Inferred relationship Some
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 muscle of shoulder (disorder) Inferred relationship Some

This concept is not in any reference sets

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