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88923002: Progressive muscular atrophy (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
147444011 Progressive muscular atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
147445012 Duchenne-Aran muscular atrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
147446013 Pure progressive muscular atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
831709012 Progressive muscular atrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1235395016 PMA - Progressive muscular atrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
72381000077116 atrophie musculaire progressive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
186951000172119 amyotrophie progressive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3436001001000116 Progressive Muskelatrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Progressive muscular atrophy Is a Motor neuron disease true Inferred relationship Some
Progressive muscular atrophy Finding site Structure of nervous system (body structure) false Inferred relationship Some 1
Progressive muscular atrophy Finding site Motor neuron false Inferred relationship Some
Progressive muscular atrophy Associated morphology Atrophy false Inferred relationship Some 1
Progressive muscular atrophy Associated morphology dégénérescence false Inferred relationship Some 2
Progressive muscular atrophy Is a Degenerative disorder true Inferred relationship Some
Progressive muscular atrophy Is a Neurological lesion false Inferred relationship Some
Progressive muscular atrophy Associated morphology Atrophy true Inferred relationship Some 1
Progressive muscular atrophy Finding site Structure of nervous system (body structure) true Inferred relationship Some 1
Progressive muscular atrophy Is a Chronic nervous system disorder true Inferred relationship Some
Progressive muscular atrophy Clinical course Progressive true Inferred relationship Some 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Post poliomyelitis syndrome Is a True Progressive muscular atrophy Inferred relationship Some
A rare genetic neurodegenerative disease characterized by neonatal to infantile onset of hypotonia, developmental delay, regression of motor skills with distal amyotrophy, ataxia, and spasticity, absent speech or dysarthria, and moderate to severe cognitive impairment. Optic atrophy may also be associated. Brain imaging shows cerebellar atrophy and thin corpus callosum, as well as brain iron accumulation in the pallidum and substantia nigra beginning during the second decade of life. Is a True Progressive muscular atrophy Inferred relationship Some

This concept is not in any reference sets

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