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86044005: Amyotrophic lateral sclerosis (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
142653015 Amyotrophic lateral sclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
142654014 Bulbar motor neuron disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
142655010 Lou Gehrig's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
506902010 ALS - Amyotrophic lateral sclerosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
828225019 Amyotrophic lateral sclerosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
142653015 Amyotrophic lateral sclerosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
142653015 Amyotrophic lateral sclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
142654014 Bulbar motor neuron disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
142654014 Bulbar motor neuron disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
142655010 Lou Gehrig's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
506902010 ALS - Amyotrophic lateral sclerosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
828225019 Amyotrophic lateral sclerosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
828225019 Amyotrophic lateral sclerosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
949831000195113 sclerosi laterale amiotrofica it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3428671001000115 Amyotrophe Lateralsklerose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
224631000172119 sclérose latérale amyotrophique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
849371000241111 SLA - sclérose latérale amyotrophique fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
849381000241113 maladie de Lou Gehrig fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
224631000172119 sclérose latérale amyotrophique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
849371000241111 SLA - sclérose latérale amyotrophique fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
849381000241113 maladie de Lou Gehrig fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
949831000195113 sclerosi laterale amiotrofica it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3428671001000115 Amyotrophe Lateralsklerose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


24 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amyotrophic lateral sclerosis Is a Motor neuron disease true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis Finding site Motor neuron (cell) false Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 2
Amyotrophic lateral sclerosis Finding site Nervous system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Amyotrophic lateral sclerosis with dementia Is a True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept)
Family history of amyotrophic lateral sclerosis (situation) Associated finding False Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of amyotrophic lateral sclerosis (situation) Associated finding True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of amyotrophic lateral sclerosis (situation) Associated finding False Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Restrictive lung disease due to amyotrophic lateral sclerosis (disorder) Due to True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept) 1
Juvenile amyotrophic lateral sclerosis Is a True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis plus syndrome (disorder) Is a True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 4 Is a True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder) Is a True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 1 Is a True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 3 Is a True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 6 Is a True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept)
A neurodegenerative disease with characteristics of progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord. Cytogenetic location is 20p13. Is a True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept)
A neurodegenerative disease with characteristics of progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord. Caused by heterozygous mutation in the VAPB gene on chromosome 20q13. Is a True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 9 Is a True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 10 Is a True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis with parkinsonism Is a True Amyotrophic lateral sclerosis Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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