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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 Reference Sets
3763685016 Amyotrophic lateral sclerosis type 4 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
3763686015 ALS4 - amyotrophic lateral sclerosis type 4 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
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 GB English: Acceptable (foundation metadata concept)
3763688019 Amyotrophic lateral sclerosis type 4 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
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 GB English: Preferred (foundation metadata concept)

0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amyotrophic lateral sclerosis type 4 Associated morphology Degeneration false Inferred relationship Some 1
Amyotrophic lateral sclerosis type 4 Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Amyotrophic lateral sclerosis type 4 Is a Amyotrophic lateral sclerosis true Inferred relationship Some
Amyotrophic lateral sclerosis type 4 Finding site Structure of central nervous system (body structure) true Inferred relationship Some 1
Amyotrophic lateral sclerosis type 4 Is a Hereditary disorder of nervous system false Inferred relationship Some
Amyotrophic lateral sclerosis type 4 Is a Degenerative disease of the central nervous system false Inferred relationship Some
Amyotrophic lateral sclerosis type 4 Is a Chronic nervous system disorder (disorder) true Inferred relationship Some
Amyotrophic lateral sclerosis type 4 Clinical course Progressive (qualifier value) true Inferred relationship Some 2
Amyotrophic lateral sclerosis type 4 Is a Hereditary degenerative disease of central nervous system true Inferred relationship Some
Amyotrophic lateral sclerosis type 4 Associated morphology Degenerative abnormality true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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