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1204351003: Amyotrophic lateral sclerosis type 9 (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4953826013 Amyotrophic lateral sclerosis type 9 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4953827016 ALS9 - amyotrophic lateral sclerosis type 9 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4953828014 Amyotrophic lateral sclerosis type 9 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4953829018 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 angiogenin gene (ANG) on chromosome 14q11. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4953826013 Amyotrophic lateral sclerosis type 9 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4953827016 ALS9 - amyotrophic lateral sclerosis type 9 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4953828014 Amyotrophic lateral sclerosis type 9 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4953829018 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 angiogenin gene (ANG) on chromosome 14q11. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amyotrophic lateral sclerosis type 9 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 9 Is a Chronic nervous system disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 9 Is a Degenerative disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 9 Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 9 Is a Amyotrophic lateral sclerosis true Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis type 9 Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2
Amyotrophic lateral sclerosis type 9 Finding site Nervous system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Amyotrophic lateral sclerosis type 9 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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