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1303912008: Congenital retained medullary spinal cord (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5308415016 Congenital retained medullary spinal cord en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5308416015 Retained medullary cord en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5308417012 Congenital retained medullary spinal cord (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5308420016 A rare closed dysraphism with terminal stalk with characteristics of persistant rudimentary spinal cord below conus. It contains non-functional neural tissue and is typically isolated. The diagnostic is suggested by attenuated conus without fat, further confirmed by pathological analysis (glioneuronal core with ependyma-lined lumen, nerve roots, and dorsal root ganglia). Differential diagnostic with intraoperative neurophysiological monitoring is mandatory as neuroimaging fails to distinguish it from functional conus. 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
Congenital retained medullary spinal cord Is a Structural developmental anomalies of neurenteric canal (disorder) true Inferred relationship Some
Congenital retained medullary spinal cord Is a Congenital anomaly of spinal cord (disorder) true Inferred relationship Some
Congenital retained medullary spinal cord Occurrence Congenital true Inferred relationship Some 1
Congenital retained medullary spinal cord Finding site Structure of conus medullaris true Inferred relationship Some 1
Congenital retained medullary spinal cord Associated morphology Persistent embryonic structure true Inferred relationship Some 1
Congenital retained medullary spinal cord Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital retained medullary spinal cord Occurrence Congenital true Inferred relationship Some 2
Congenital retained medullary spinal cord Finding site Neurenteric canal true Inferred relationship Some 2
Congenital retained medullary spinal cord Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Congenital retained medullary spinal cord Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Congenital retained medullary spinal cord Is a Neural tube defect true Inferred relationship Some
Congenital retained medullary spinal cord Occurrence Congenital true Inferred relationship Some 3
Congenital retained medullary spinal cord Finding site Neural tube structure true Inferred relationship Some 3
Congenital retained medullary spinal cord Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Congenital retained medullary spinal cord Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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