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128208007: Peripheral axonal neuropathy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
206450013 Peripheral axonal neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
732173015 Peripheral axonal neuropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
304341000077114 neuropathie axonale périphérique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
310811000172118 neuropathie périphérique axonale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Peripheral axonal neuropathy Is a Axonal neuropathy true Inferred relationship Some
Peripheral axonal neuropathy Finding site Nerve structure false Inferred relationship Some
Peripheral axonal neuropathy Finding site Peripheral nervous system structure false Inferred relationship Some
Peripheral axonal neuropathy Is a Disorder of the peripheral nervous system false Inferred relationship Some
Peripheral axonal neuropathy Is a Peripheral nerve disease true Inferred relationship Some
Peripheral axonal neuropathy Finding site Peripheral nerve structure true Inferred relationship Some 1
Peripheral axonal neuropathy Finding site Axon structure true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal recessive axonal neuropathy with neuromyotonia Is a True Peripheral axonal neuropathy Inferred relationship Some
A rare syndromic neurological disorder characterized by the association of Möbius syndrome (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. There have been no further reports since 1996. Is a True Peripheral axonal neuropathy Inferred relationship Some
Axonal sensorimotor neuropathy Is a True Peripheral axonal neuropathy Inferred relationship Some
A rare, genetic, autosomal recessive axonal hereditary motor and sensory neuropathy disease characterized by prenatal onset of a severe sensorimotor axonal polyneuropathy (reflected by reduced fetal movement and polyhydramnios), manifesting, at birth, with respiratory failure requiring mechanical ventilation, profound muscular hypotonia, rapidly progressing distal muscle weakness, and absent deep tendon reflexes, in the absence of contractures, leading to death before 8 months of age. Neuropathological findings show severe loss of large- and medium-sized myelinated fibers without signs of demyelination. Is a True Peripheral axonal neuropathy Inferred relationship Some
Atrophy of axon of peripheral nerve structure (disorder) Is a True Peripheral axonal neuropathy Inferred relationship Some

This concept is not in any reference sets

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