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69106008: Congenital failure of fusion with herniated tissue (morphologic abnormality)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    114782016 Congenital failure of fusion with herniated tissue en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    114783014 Congenital defective closure with herniation of tissue en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    809015018 Congenital failure of fusion with herniated tissue (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    114782016 Congenital failure of fusion with herniated tissue en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    114782016 Congenital failure of fusion with herniated tissue en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    114783014 Congenital defective closure with herniation of tissue en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    114783014 Congenital defective closure with herniation of tissue en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    809015018 Congenital failure of fusion with herniated tissue (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    809015018 Congenital failure of fusion with herniated tissue (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital failure of fusion with herniated tissue Is a Congenital failure of fusion false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital failure of fusion with herniated tissue Is a Congenital protrusion false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital failure of fusion with herniated tissue Is a Developmental failure of fusion (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept)

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Nasal encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Nasal encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 3
    Congenital spinal hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital spinal hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 3
    hydroméningocèle crânienne congénitale Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    hydroméningocèle crânienne congénitale Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Repair of meningoencephalocele Direct morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    Repair of meningoencephalocele Direct morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Thoracic hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    Thoracic hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Spina bifida of lumbar region (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital cerebral meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    hydroméningocèle Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    [X]Encephalocele of other sites Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Cervical spinal meningocele (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Temporal encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    Meningoencephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hydrencephalomeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Frontoethmoidal encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Parietal encephalocele (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    Encephalocele of orbit Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    Frontal encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Meningomyelocele/myelocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 3
    hydromyéloméningocèle Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 3
    hernie endo-auriculaire congénitale Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital cerebral hernia Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    encéphalocystocèle Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Occipital encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    Encephalocele of other specified site Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Lumbar spina bifida with hydrocephalus - closed Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Encephalocele NOS Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Encephalomyelocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital sacral meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Lumbar spina bifida without hydrocephalus - closed Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Repair of encephalocele Direct morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Myelocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    Encephalocystocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Cervical spinal hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Spinal meningocele of unspecified site Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 3
    Thoracic spinal meningocele (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Lumbar spinal meningocele (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Spinal meningocele NOS Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 3
    Myelocele NOS Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    Spinal meningocele NOS Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 3
    Spinal meningocele of unspecified site Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 3
    Myelocele of unspecified site Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    Spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Thoracic spinal meningocele (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Thoracic myelocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 4
    Lumbar spinal meningocele (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Cervical spinal meningocele (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Lumbar myelocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 4
    Cervical myelocele (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 4
    Cervical spinal hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Encephalocele of vertex (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Known OR suspected fetal spina bifida with myelomeningocele affecting obstetrical care Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Known OR suspected fetal spina bifida with myelomeningocele affecting obstetrical care Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Encephalocele of vertex (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Myelocele with hydrocephalus Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Cervical spinal hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 4
    Retinal detachment and occipital encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 8
    Congenital laryngocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 3
    Congenital laryngocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 6
    Congenital spinal hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 9
    DK phocomelia syndrome (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 6
    Thoracic spinal meningocele (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 3
    Spina bifida and hypospadias syndrome Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Spina bifida and hypospadias syndrome Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    Retinal detachment and occipital encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 5
    Encephalocystocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    DK phocomelia syndrome (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 3
    Encephalocele of orbit Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital spinal hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 5
    Congenital cerebral meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Zechi Ceide syndrome Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 5
    A rare genetic bone development disorder characterized by occipital and parietal bone hypoplasia leading to occipital encephalocele, calvarial mineralization defects, craniosynostosis, radiohumeral fusions, oligodactyly and other skeletal anomalies (arachnodactyly, terminal phalangeal aplasia of the thumbs, bilateral absence of the great toes, pronounced bilateral angulation of femora, shortened limbs, advanced osseous maturation). Fetal death in utero is associated. There is evidence the disease can be caused by homozygous mutation in the CYP26B1 gene on chromosome 2p13. Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 1
    Meningoencephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 2
    Myelocele with hydrocephalus Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Existential restriction modifier (core metadata concept) 4

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