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784341001: Amyotrophic lateral sclerosis type 4 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3763685016 Amyotrophic lateral sclerosis type 4 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763686015 ALS4 - amyotrophic lateral sclerosis type 4 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3763687012 dHMN (distal hereditary motor neuropathy) with upper motor neuron signs en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3763688019 Amyotrophic lateral sclerosis type 4 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763689010 A rare genetic motor neuron disease with characteristics of late childhood or adolescent onset of slowly progressive severe distal limb muscle weakness and wasting, in association with pyramidal signs, normal sensation and absence of bulbar involvement. Leads to degeneration of motor neurons in the brain and spinal cord. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3763685016 Amyotrophic lateral sclerosis type 4 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763686015 ALS4 - amyotrophic lateral sclerosis type 4 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3763687012 dHMN (distal hereditary motor neuropathy) with upper motor neuron signs en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3763688019 Amyotrophic lateral sclerosis type 4 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3763689010 A rare genetic motor neuron disease with characteristics of late childhood or adolescent onset of slowly progressive severe distal limb muscle weakness and wasting, in association with pyramidal signs, normal sensation and absence of bulbar involvement. Leads to degeneration of motor neurons in the brain and spinal cord. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3395761001000113 Amyotrophe Lateralsklerose Typ 4 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5947171000241111 sclérose latérale amyotrophique de type 4 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5947181000241113 maladie de Charcot de type 4 fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5947191000241110 SLA (sclérose latérale amyotrophique) de type 4 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5947171000241111 sclérose latérale amyotrophique de type 4 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5947181000241113 maladie de Charcot de type 4 fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5947191000241110 SLA (sclérose latérale amyotrophique) de type 4 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3395761001000113 Amyotrophe Lateralsklerose Typ 4 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amyotrophic lateral sclerosis type 4 Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyotrophic lateral sclerosis type 4 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 4 Is a Amyotrophic lateral sclerosis true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 4 Finding site Structure of central nervous system true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyotrophic lateral sclerosis type 4 Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 4 Is a Degenerative disease of the central nervous system false Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 4 Is a Chronic nervous system disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 4 Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2
Amyotrophic lateral sclerosis type 4 Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 4 Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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