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1303445002: Myelic limited dorsal malformation (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
5306487012 Myelic limited dorsal malformation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5306488019 Myelic limited dorsal malformation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5306489010 MyeLDM - myelic limited dorsal malformation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5306491019 A rare intermediate form of open dysraphism between myelomeningocele and saccular limited dorsal myeloschisis without fulfilling the characteristics of one of these two diagnosis, characterized by stretched neurulation of spinal cord attached at the dome of a sac. Partial cerebral signs of open dysraphism can be observed and the meningocele is usually poorly epithelialized. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5306492014 A rare intermediate form of open dysraphism between myelomeningocele and saccular limited dorsal myeloschisis without fulfilling the characteristics of one of these two diagnosis, characterised by stretched neurulation of spinal cord attached at the dome of a sac. Partial cerebral signs of open dysraphism can be observed and the meningocele is usually poorly epithelialised. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5306487012 Myelic limited dorsal malformation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5306488019 Myelic limited dorsal malformation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5306489010 MyeLDM - myelic limited dorsal malformation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5306491019 A rare intermediate form of open dysraphism between myelomeningocele and saccular limited dorsal myeloschisis without fulfilling the characteristics of one of these two diagnosis, characterized by stretched neurulation of spinal cord attached at the dome of a sac. Partial cerebral signs of open dysraphism can be observed and the meningocele is usually poorly epithelialized. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5306492014 A rare intermediate form of open dysraphism between myelomeningocele and saccular limited dorsal myeloschisis without fulfilling the characteristics of one of these two diagnosis, characterised by stretched neurulation of spinal cord attached at the dome of a sac. Partial cerebral signs of open dysraphism can be observed and the meningocele is usually poorly epithelialised. 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
Myelic limited dorsal malformation Is a Congenital meningocele true Inferred relationship Existential restriction modifier (core metadata concept)
Myelic limited dorsal malformation Is a Structural developmental anomalies of neurenteric canal (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Myelic limited dorsal malformation Is a Neural tube defect true Inferred relationship Existential restriction modifier (core metadata concept)
Myelic limited dorsal malformation Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Myelic limited dorsal malformation Finding site Meninges structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Myelic limited dorsal malformation Associated morphology Herniated structure (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Myelic limited dorsal malformation Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Myelic limited dorsal malformation Finding site Neurenteric canal true Inferred relationship Existential restriction modifier (core metadata concept) 2
Myelic limited dorsal malformation Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Myelic limited dorsal malformation Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Myelic limited dorsal malformation Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Myelic limited dorsal malformation Finding site Neural tube structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Myelic limited dorsal malformation Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Myelic limited dorsal malformation Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

Description inactivation indicator reference set

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