FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.7  |  FHIR Version n/a  User: [n/a]

1119329003: Progressive peripheral neuropathy (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Aug 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4361562019 Progressive peripheral neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4361563012 Progressive peripheral neuropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

14 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Progressive peripheral neuropathy Is a Chronic nervous system disorder (disorder) true Inferred relationship Some
Progressive peripheral neuropathy Is a Peripheral nerve disease true Inferred relationship Some
Progressive peripheral neuropathy Clinical course Progressive (qualifier value) true Inferred relationship Some 1
Progressive peripheral neuropathy Finding site Peripheral nerve structure true Inferred relationship Some 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Progressive symmetric demyelination of peripheral nerve (disorder) Is a True Progressive peripheral neuropathy Inferred relationship Some
Hemifacial spasm Is a True Progressive peripheral neuropathy Inferred relationship Some
Progressive polyneuropathy with bilateral striatal necrosis Is a True Progressive peripheral neuropathy Inferred relationship Some
Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome (disorder) Is a True Progressive peripheral neuropathy Inferred relationship Some
Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 (disorder) Is a True Progressive peripheral neuropathy Inferred relationship Some
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation Is a True Progressive peripheral neuropathy Inferred relationship Some
Cerebellar ataxia with oculomotor apraxia type 4 (disorder) Is a True Progressive peripheral neuropathy Inferred relationship Some
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) Is a True Progressive peripheral neuropathy Inferred relationship Some
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome Is a True Progressive peripheral neuropathy Inferred relationship Some
Mitchell syndrome Is a True Progressive peripheral neuropathy Inferred relationship Some
Polyneuropathy associated with immunoglobulin M monoclonal gammopathy of uncertain significance (disorder) Is a True Progressive peripheral neuropathy Inferred relationship Some

Reference Sets

GB English

US English

Back to Start