54280009: Kugelberg-Welander disease (disorder)

SNOMED CT Concept\Clinical finding\Disease\...

\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Kugelberg-Welander disease

\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Kugelberg-Welander disease
\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Kugelberg-Welander disease
\Disorder of body system\Disorder of nervous system\Motor neuron disease\Lower motor neuron disease\Spinal muscular atrophy\Kugelberg-Welander disease
\Disorder of body system\Disorder of nervous system\Motor neuron disease\Hereditary motor neuron disease\Spinal muscular atrophy\Kugelberg-Welander disease

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

90227012 Kugelberg-Welander disease en Synonym Active Entire term case sensitive SNOMED CT core module
90228019 Familial spinal muscular atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
90229010 Juvenile spinal muscular atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
198509013 Spinal muscular atrophy, type III en Synonym Active Only initial character case insensitive SNOMED CT core module
198510015 SMA3 en Synonym Active Entire term case sensitive SNOMED CT core module
198511016 SMA type III en Synonym Active Entire term case sensitive SNOMED CT core module
792493019 Kugelberg-Welander disease (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1231316010 Spinal muscular atrophy type III en Synonym Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Kugelberg-Welander disease	Is a	Spinal muscular atrophy	true	Inferred relationship	Existential restriction modifier
Kugelberg-Welander disease	Associated morphology	Degeneration	false	Inferred relationship	Existential restriction modifier	2
Kugelberg-Welander disease	Finding site	Motor neuron	false	Inferred relationship	Existential restriction modifier
Kugelberg-Welander 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