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249491000119100: Structural developmental anomalies of neurenteric canal (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3004433015 Spinal dysraphism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3008898011 Structural developmental anomalies of neurenteric canal (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009020016 Structural developmental anomalies of neurenteric canal en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3004433015 Spinal dysraphism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3004433015 Spinal dysraphism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3008898011 Structural developmental anomalies of neurenteric canal (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3008898011 Structural developmental anomalies of neurenteric canal (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3008993018 Structural developmental anomalies of neuroenteric canal en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3008993018 Structural developmental anomalies of neuroenteric canal en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009020016 Structural developmental anomalies of neurenteric canal en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3009020016 Structural developmental anomalies of neurenteric canal en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

48 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Structural developmental anomalies of neurenteric canal (disorder) Is a Congenital malformation true Inferred relationship Existential restriction modifier (core metadata concept)
Structural developmental anomalies of neurenteric canal (disorder) Is a Disorder of embryonic structure (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Structural developmental anomalies of neurenteric canal (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Structural developmental anomalies of neurenteric canal (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Structural developmental anomalies of neurenteric canal (disorder) Finding site Neurenteric canal true Inferred relationship Existential restriction modifier (core metadata concept) 1
Structural developmental anomalies of neurenteric canal (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Structural developmental anomalies of neurenteric canal (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Primary tethered cord syndrome (disorder) Is a True Structural developmental anomalies of neurenteric canal (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Spina bifida aperta Is a True Structural developmental anomalies of neurenteric canal (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Freeing of spinal tether (procedure) Has focus True Structural developmental anomalies of neurenteric canal (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 2
Repair of spinal dysraphism Has focus True Structural developmental anomalies of neurenteric canal (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 1
Lipoma due to neurospinal dysraphism Due to True Structural developmental anomalies of neurenteric canal (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 2
Dysraphism, cleft lip and palate, limb reduction defect syndrome (disorder) Is a True Structural developmental anomalies of neurenteric canal (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Isolated lipoma of filum terminale Is a True Structural developmental anomalies of neurenteric canal (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare dysraphic abnormality characterised by the infiltration of fatty tissue localised in the filum terminale, with abnormal conus shape. The spinal cord is typically attenuated and the limit between its end and the fatty filum is hard to distinguish. There is no additional spinal cord malformation, but it can be associated with vertebral abnormalities, anorectal malformation or other syndromic condition. It is named transitional for its intermediate image between an isolated filum lipoma and a terminal conus region lipoma. Is a True Structural developmental anomalies of neurenteric canal (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Myelic limited dorsal malformation Is a True Structural developmental anomalies of neurenteric canal (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Chaotic conus spinal cord lipoma Is a True Structural developmental anomalies of neurenteric canal (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare closed dysraphism with stalk characterized by a dorsal midline dermal sinus tract lined by keratinizing stratified squamous epithelium extending to the intrathecal space. Other components such as hair follicles and shafts, mesenchymal derivatives (blood vessels and fibrous tissue) and occasionally nerve fibers can be observed. Inflamed granulation tissue containing mixed neutrophils, plasma cells, lymphocytes, and histiocytes is consistently found in the tract. It can also be associated with an intradural dermoid cyst. This malformation is at risk to cause intrathecal infections (meningitis, empyema) that justify prophylactic surgery. Is a True Structural developmental anomalies of neurenteric canal (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital retained medullary spinal cord Is a True Structural developmental anomalies of neurenteric canal (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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