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64383006: Werdnig-Hoffmann disease (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
107017013 Werdnig-Hoffmann disease en Synonym Active Entire term case sensitive SNOMED CT core module
107018015 Infantile spinal muscular atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
107019011 Progressive muscular atrophy of infancy en Synonym Active Entire term case insensitive SNOMED CT core module
199235017 Spinal muscular atrophy, type I en Synonym Active Only initial character case insensitive SNOMED CT core module
803770017 Werdnig-Hoffmann disease (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1232557016 Spinal muscular atrophy type I en Synonym Active Only initial character case insensitive SNOMED CT core module
1232558014 WHD - Werdnig-Hoffmann disease en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Werdnig-Hoffmann disease Is a Spinal muscular atrophy true Inferred relationship Existential restriction modifier
Werdnig-Hoffmann disease Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Werdnig-Hoffmann disease Associated morphology Degeneration false Inferred relationship Existential restriction modifier 2
Werdnig-Hoffmann disease Finding site Motor neuron false Inferred relationship Existential restriction modifier
Werdnig-Hoffmann disease Is a Anterior horn cell disease true Inferred relationship Existential restriction modifier
Werdnig-Hoffmann disease Finding site Structure of nervous system true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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