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230256009: Benign monomelic amyotrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

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


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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