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1237626001: Congenital axonal neuropathy with encephalopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5100117019 Congenital axonal neuropathy with encephalopathy en Synonym Active Entire term case insensitive SNOMED CT core module
5100118012 Congenital axonal neuropathy with encephalopathy (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
Congenital axonal neuropathy with encephalopathy Is a Hereditary motor and sensory neuropathy true Inferred relationship Existential restriction modifier
Congenital axonal neuropathy with encephalopathy Is a Axonal neuropathy true Inferred relationship Existential restriction modifier
Congenital axonal neuropathy with encephalopathy Is a Congenital disease true Inferred relationship Existential restriction modifier
Congenital axonal neuropathy with encephalopathy Is a Disorder of brain true Inferred relationship Existential restriction modifier
Congenital axonal neuropathy with encephalopathy Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Congenital axonal neuropathy with encephalopathy Finding site Brain structure true Inferred relationship Existential restriction modifier 4
Congenital axonal neuropathy with encephalopathy Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital axonal neuropathy with encephalopathy Finding site Nerve structure true Inferred relationship Existential restriction modifier 1
Congenital axonal neuropathy with encephalopathy Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital axonal neuropathy with encephalopathy Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier 2
Congenital axonal neuropathy with encephalopathy Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Congenital axonal neuropathy with encephalopathy Finding site Axon structure true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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