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784341001: Amyotrophic lateral sclerosis type 4 (disorder)


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

Descriptions:

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


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 Existential restriction modifier 1
Amyotrophic lateral sclerosis type 4 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Amyotrophic lateral sclerosis type 4 Is a Amyotrophic lateral sclerosis true Inferred relationship Existential restriction modifier
Amyotrophic lateral sclerosis type 4 Finding site Structure of central nervous system true Inferred relationship Existential restriction modifier 1
Amyotrophic lateral sclerosis type 4 Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Amyotrophic lateral sclerosis type 4 Is a Degenerative disease of the central nervous system false Inferred relationship Existential restriction modifier
Amyotrophic lateral sclerosis type 4 Is a Chronic nervous system disorder true Inferred relationship Existential restriction modifier
Amyotrophic lateral sclerosis type 4 Clinical course Progressive true Inferred relationship Existential restriction modifier 2
Amyotrophic lateral sclerosis type 4 Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Amyotrophic lateral sclerosis type 4 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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