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230256009: Benign monomelic amyotrophy (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
345073018 Benign monomelic amyotrophy en Synonym Active Case insensitive SNOMED CT core
618038016 Benign monomelic amyotrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Benign monomelic amyotrophy Is a Chronic nervous system disorder true Inferred relationship Some
Benign monomelic amyotrophy Is a Chronic disease of musculoskeletal system true Inferred relationship Some
Benign monomelic amyotrophy Clinical course Progressive true Inferred relationship Some 3
Benign monomelic amyotrophy Finding site Skeletal muscle structure true Inferred relationship Some 1
Benign monomelic amyotrophy Associated morphology Atrophy true Inferred relationship Some 1
Benign monomelic amyotrophy Is a Neurological disorder false Inferred relationship Some
Benign monomelic amyotrophy Is a Muscle atrophy true Inferred relationship Some
Benign monomelic amyotrophy Finding site Structure of nervous system true Inferred relationship Some 2
Benign monomelic amyotrophy Finding site Skeletal muscle structure false Inferred relationship Some 1
Benign monomelic amyotrophy Associated morphology Atrophy false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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