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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
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 Some
Congenital meningocele Occurrence Congenital false Inferred relationship Some
Congenital meningocele Finding site The three membranes that surround the brain and spinal cord, consisting of the dura mater, arachnoid, and pia mater. The pia and arachnoid in combination are referred to as the leptomeninges. false Inferred relationship Some 1
Congenital meningocele Is a Congenital disease false Inferred relationship Some
Congenital meningocele Associated morphology Herniated structure (morphologic abnormality) false Inferred relationship Some 1
Congenital meningocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Some 2
Congenital meningocele Finding site Bone structure false Inferred relationship Some 2
Congenital meningocele Is a Congenital connective tissue disorder false Inferred relationship Some
Congenital meningocele Associated morphology Herniated structure (morphologic abnormality) true Inferred relationship Some 1
Congenital meningocele Finding site The three membranes that surround the brain and spinal cord, consisting of the dura mater, arachnoid, and pia mater. The pia and arachnoid in combination are referred to as the leptomeninges. false Inferred relationship Some 1
Congenital meningocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Some 2
Congenital meningocele Finding site Bone structure false Inferred relationship Some 2
Congenital meningocele Is a Congenital disease true Inferred relationship Some
Congenital meningocele Associated morphology Protrusion false Inferred relationship Some 1
Congenital meningocele Finding site The three membranes that surround the brain and spinal cord, consisting of the dura mater, arachnoid, and pia mater. The pia and arachnoid in combination are referred to as the leptomeninges. true Inferred relationship Some 1
Congenital meningocele Associated morphology Protrusion false Inferred relationship Some 1
Congenital meningocele Occurrence Congenital false Inferred relationship Some 2
Congenital meningocele Finding site The three membranes that surround the brain and spinal cord, consisting of the dura mater, arachnoid, and pia mater. The pia and arachnoid in combination are referred to as the leptomeninges. false Inferred relationship Some 2
Congenital meningocele Is a Congenital malformation of the meninges false Inferred relationship Some
Congenital meningocele Associated morphology Congenital protrusion false Inferred relationship Some 2
Congenital meningocele Occurrence Congenital true Inferred relationship Some 1
Congenital meningocele Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
A type of spina bifida aperta that is usually caused by a vertebral defect associated with a superficial fatty mass (lipoma or fatty tumour) that merges with the lower level of the spinal cord. Is a False Congenital meningocele Inferred relationship Some
Lateral meningocele Is a True Congenital meningocele Inferred relationship Some
hydroméningocèle Is a False Congenital meningocele Inferred relationship Some
Congenital cerebral meningocele Is a True Congenital meningocele Inferred relationship Some
Congenital spinal meningocele Is a True Congenital meningocele Inferred relationship Some
hydromyéloméningocèle Is a False Congenital meningocele Inferred relationship Some
Congenital sacral meningocele Is a True Congenital meningocele Inferred relationship Some
Occipital meningocele (disorder) Is a True Congenital meningocele Inferred relationship Some
Thoracic hydromeningocele Is a False Congenital meningocele Inferred relationship Some
A rare syndromic central nervous system malformation characterized 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 Some
Posterior meningocele is a rare neural tube closure defect characterized by the herniation of a cerebrospinal fluid-filled sac, that is lined by dura and arachnoid mater, through a posterior spina bifida and covered by a layer of skin of variable thickness, which may be dysplastic or ulcerated. The spinal cord and nerves are generally not included and function normally, although sometimes a tethered cord may be associated. They are most commonly located in the lumbar or sacral region. Is a True Congenital meningocele Inferred relationship Some
Congenital meningocele of orbit (disorder) Is a True Congenital meningocele Inferred relationship Some
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. Is a True Congenital meningocele Inferred relationship Some

This concept is not in any reference sets

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