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172069000: Congenital meningocele (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
266440018 Congenital meningocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
266441019 Congenital hernia of dura mater en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
554208010 Congenital meningocele (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4571995013 Congenital hydromeningocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
266440018 Congenital meningocele en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
266440018 Congenital meningocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
266441019 Congenital hernia of dura mater en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
266441019 Congenital hernia of dura mater en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
266442014 Congenital meningocele, NOS en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
266443016 Meningocele, NOS en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
554208010 Congenital meningocele (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
554208010 Congenital meningocele (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4571995013 Congenital hydromeningocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6926871000241119 méningocèle congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6926871000241119 méningocèle congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

24 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital meningocele Is a Meningocele true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital meningocele Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital meningocele Finding site Meninges structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital meningocele Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital meningocele Associated morphology Herniated structure (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital meningocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital meningocele Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital meningocele Is a Congenital connective tissue disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital meningocele Associated morphology Herniated structure (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital meningocele Finding site Meninges structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital meningocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital meningocele Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital meningocele Is a Congenital disease true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital meningocele Associated morphology Protrusion false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital meningocele Finding site Meninges structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital meningocele Associated morphology Protrusion false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital meningocele Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital meningocele Finding site Meninges structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital meningocele Is a Congenital malformation of the meninges false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital meningocele Associated morphology Congenital protrusion false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital meningocele Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital meningocele Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Lipomeningocele (disorder) Is a False Congenital meningocele Inferred relationship Existential restriction modifier (core metadata concept)
Lateral meningocele Is a True Congenital meningocele Inferred relationship Existential restriction modifier (core metadata concept)
hydroméningocèle Is a False Congenital meningocele Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebral meningocele Is a True Congenital meningocele Inferred relationship Existential restriction modifier (core metadata concept)
Congenital spinal meningocele Is a True Congenital meningocele Inferred relationship Existential restriction modifier (core metadata concept)
hydromyéloméningocèle Is a False Congenital meningocele Inferred relationship Existential restriction modifier (core metadata concept)
Congenital sacral meningocele Is a True Congenital meningocele Inferred relationship Existential restriction modifier (core metadata concept)
Occipital meningocele (disorder) Is a True Congenital meningocele Inferred relationship Existential restriction modifier (core metadata concept)
Thoracic hydromeningocele Is a False Congenital meningocele Inferred relationship Existential restriction modifier (core metadata concept)
A rare syndromic central nervous system malformation characterised by the association of conotruncal heart defects, myelomeningocele and craniofacial dysmorphism similar to that seen in monosomy 22q11. Is a False Congenital meningocele Inferred relationship Existential restriction modifier (core metadata concept)
Posterior meningocele Is a True Congenital meningocele Inferred relationship Existential restriction modifier (core metadata concept)
Congenital meningocele of orbit (disorder) Is a True Congenital meningocele Inferred relationship Existential restriction modifier (core metadata concept)
Myelic limited dorsal malformation Is a True Congenital meningocele Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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