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1263540002: Benign monomelic amyotrophy of upper limb (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5169032014 Monomelic amyotrophy of upper limb en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5169033016 Benign monomelic amyotrophy of upper limb (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5169595018 Benign monomelic amyotrophy of upper limb en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Benign monomelic amyotrophy of upper limb (disorder) Is a Disorder of upper limb (disorder) true Inferred relationship Some
Benign monomelic amyotrophy of upper limb (disorder) Is a Benign monomelic amyotrophy true Inferred relationship Some
Benign monomelic amyotrophy of upper limb (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 2
Benign monomelic amyotrophy of upper limb (disorder) Finding site Structure of nervous system (body structure) true Inferred relationship Some 3
Benign monomelic amyotrophy of upper limb (disorder) Finding site Skeletal muscle structure of upper limb true Inferred relationship Some 1
Benign monomelic amyotrophy of upper limb (disorder) Associated morphology Atrophy 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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