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76916001: Spina bifida occulta (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
127701015 Spina bifida occulta en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
127702010 Cryptomerorachischisis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
817689015 Spina bifida occulta (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1234043013 SBO - Spina bifida occulta en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4279490017 A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
127701015 Spina bifida occulta en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
127701015 Spina bifida occulta en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
127702010 Cryptomerorachischisis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
127702010 Cryptomerorachischisis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
817689015 Spina bifida occulta (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
817689015 Spina bifida occulta (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1234043013 SBO - Spina bifida occulta en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1234043013 SBO - Spina bifida occulta en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4279490017 A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
229451000172110 spina bifida occulte fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
641201000172111 spina bifida occulta fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
229451000172110 spina bifida occulte fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
641201000172111 spina bifida occulta fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


18 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Is a Spina bifida true Inferred relationship Existential restriction modifier (core metadata concept)
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Finding site Bone structure of spine false Inferred relationship Existential restriction modifier (core metadata concept) 2
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Finding site Sacral spine structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Associated morphology Congenital failure of fusion false Inferred relationship Existential restriction modifier (core metadata concept) 2
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Is a Disorder of back false Inferred relationship Existential restriction modifier (core metadata concept)
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier (core metadata concept)
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Is a Sacral spine finding false Inferred relationship Existential restriction modifier (core metadata concept)
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Finding site Neural tube structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 3
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 3
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Finding site Structure of arch of vertebra false Inferred relationship Existential restriction modifier (core metadata concept) 2
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Finding site Neural tube structure false Inferred relationship Existential restriction modifier (core metadata concept) 5
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Finding site Structure of arch of vertebra false Inferred relationship Existential restriction modifier (core metadata concept) 2
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Associated morphology Congenital failure of fusion false Inferred relationship Existential restriction modifier (core metadata concept) 2
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 4
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Finding site Structure of vertebral column false Inferred relationship Existential restriction modifier (core metadata concept) 4
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 5
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Associated morphology Developmental failure of fusion (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Finding site Structure of arch of vertebra true Inferred relationship Existential restriction modifier (core metadata concept) 1
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Finding site Neural tube structure true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Split spinal cord malformation (disorder) Is a False A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Inferred relationship Existential restriction modifier (core metadata concept)
Spina bifida with hydrocephalus - closed Is a True A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Inferred relationship Existential restriction modifier (core metadata concept)
Spina bifida without hydrocephalus - closed Is a True A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Inferred relationship Existential restriction modifier (core metadata concept)
Occult spinal dysraphism sequence Is a True A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Inferred relationship Existential restriction modifier (core metadata concept)
Closed spina bifida with Arnold-Chiari malformation (disorder) Is a True A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Inferred relationship Existential restriction modifier (core metadata concept)
Faun tail syndrome Is a True A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges. Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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