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3058005: Peripheral nervous system structure (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
6178013 Peripheral nervous system en Synonym Active Entire term case insensitive SNOMED CT core module
484640017 Peripheral nervous system structure en Synonym Active Entire term case insensitive SNOMED CT core module
761600011 Peripheral nervous system structure (body structure) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2579326017 PNS - Peripheral nervous system en Synonym Active Entire term case sensitive SNOMED CT core module


1775 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Peripheral nervous system structure Is a Entire subdivision of nervous system false Inferred relationship Existential restriction modifier
Peripheral nervous system structure Part of Entire nervous system false Additional relationship Existential restriction modifier
Peripheral nervous system structure Is a Structure of nervous system false Inferred relationship Existential restriction modifier
Peripheral nervous system structure Is a Structure of subdivision of nervous system true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
X-linked distal arthrogryposis multiplex congenita Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 3
Autosomal dominant Charcot-Marie-Tooth disease type 2W Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Hereditary sensory and autonomic neuropathy type 8 Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 3
Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 1 Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 1
Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 3
Charcot-Marie-Tooth disease type 2T Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Autosomal recessive Charcot-Marie-Tooth disease type 2X Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2Z Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Autosomal dominant Charcot-Marie-Tooth disease type 2Y Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to trafficking from endoplasmic reticulum to golgi regulator mutation Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Autosomal recessive intermediate Charcot-Marie-Tooth disease type D Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 1
Charcot-Marie-Tooth disease type 2S Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Autosomal dominant Charcot-Marie-Tooth disease type 2V Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2DD Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
DnaJ heat shock protein family (Hsp40) member B2-related Charcot-Marie-Tooth disease type 2 Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 4
Distal hereditary motor neuropathy type 5 Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Neurogenic scapuloperoneal syndrome Kaeser type Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 3
Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 5
Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 3
Distal hereditary motor neuropathy type 2 Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 3
Congenital insensitivity to pain with severe intellectual disability Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Congenital axonal neuropathy with encephalopathy Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Hereditary sensory autonomic neuropathy type IIC Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Polyendocrine polyneuropathy syndrome Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
[X]Polyneuropathy in neoplastic disease classified elsewhere Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
[X]Other mononeuropathies in diseases classified elsewhere Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
[X]Polyneuropathy in nutritional deficiency classified elsewhere Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
[X]Other specified mononeuropathies Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Disorder of muscle tone of newborn Finding site True Peripheral nervous system structure Inferred relationship Existential restriction modifier 2
Other specified disorders of peripheral nervous system Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Peripheral nervous system disorder NOS Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Trigeminal neuralgia [no drugs here] Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Neuralgia, neuritis and radiculitis unspecified Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Neuralgia unspecified Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Radiculitis unspecified Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Mononeuritis of unspecified site NOS Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Other idiopathic peripheral neuropathy Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Other idiopathic peripheral neuropathy NOS Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Peroneal muscular atrophy NOS Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Neuralgia, neuritis or radiculitis NOS Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Trigeminal neuralgia NOS Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Other specified trigeminal neuralgia Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Hereditary peripheral neuropathy NOS Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Algoneurodystrophy NOS Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Disorder of muscle tone of newborn Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier 3
Symptomatic diabetic peripheral neuropathy Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier
Disorder of muscle tone of newborn Finding site False Peripheral nervous system structure Inferred relationship Existential restriction modifier

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