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784341001: Amyotrophic lateral sclerosis type 4 (disorder)


Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3763685016 Amyotrophic lateral sclerosis type 4 en Synonym Active Case insensitive SNOMED CT core
3763686015 ALS4 - amyotrophic lateral sclerosis type 4 en Synonym Active Case sensitive SNOMED CT core
3763687012 dHMN (distal hereditary motor neuropathy) with upper motor neuron signs en Synonym Active Case sensitive SNOMED CT core
3763688019 Amyotrophic lateral sclerosis type 4 (disorder) en Fully specified name Active Case insensitive 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 Case sensitive SNOMED CT core


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 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 true Inferred relationship Some
Amyotrophic lateral sclerosis type 4 Clinical course Progressive 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

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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