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4919007: Congenital protrusion (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
    9204016 Congenital protrusion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    9209014 Congenital hernia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    9210016 Congenital herniation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    9211017 Congenital evagination en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    786841010 Congenital protrusion (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    28011000052113 kongenital protrusion sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    kongenital protrusion Is a kongenital anomali false Inferred relationship Some
    kongenital protrusion Is a medfödd missbildning false Inferred relationship Some
    kongenital protrusion Is a Protrusion false Inferred relationship Some
    kongenital protrusion Is a utvecklingsabnormitet false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    kranialt hydromeningocele Associated morphology False kongenital protrusion Inferred relationship Some 7
    Retinal detachment and occipital encephalocele Associated morphology False kongenital protrusion Inferred relationship Some 7
    Thoracic spinal meningocele Associated morphology False kongenital protrusion Inferred relationship Some 5
    Cervical spinal meningocele Associated morphology False kongenital protrusion Inferred relationship Some 5
    Lumbar spinal meningocele (disorder) Associated morphology False kongenital protrusion Inferred relationship Some 5
    Congenital mesocolic hernia Associated morphology False kongenital protrusion Inferred relationship Some 1
    Maxillary prognathism Associated morphology False kongenital protrusion Inferred relationship Some 5
    Congenital prognathism Associated morphology False kongenital protrusion Inferred relationship Some 4
    Mandibular prognathism Associated morphology False kongenital protrusion Inferred relationship Some 5
    Congenital spinal meningocele Associated morphology False kongenital protrusion Inferred relationship Some 5
    Hydrocephalus due to Arnold Chiari malformation type 2 Associated morphology False kongenital protrusion Inferred relationship Some 2
    Cervical spinal meningocele Associated morphology False kongenital protrusion Inferred relationship Some 7
    Lumbar spinal meningocele (disorder) Associated morphology False kongenital protrusion Inferred relationship Some 7
    medfött spinalt hydromeningocele Associated morphology False kongenital protrusion Inferred relationship Some 8
    Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome (disorder) Associated morphology False kongenital protrusion Inferred relationship Some 5
    Shprintzen Goldberg omphalocele syndrome (disorder) Associated morphology False kongenital protrusion Inferred relationship Some 9
    Lethal omphalocele with cleft palate syndrome (disorder) Associated morphology False kongenital protrusion Inferred relationship Some 11
    Congenital sacral meningocele Associated morphology False kongenital protrusion Inferred relationship Some 5
    Thoracic spinal meningocele Associated morphology False kongenital protrusion Inferred relationship Some 2
    Capra DeMarco syndrome (disorder) Associated morphology False kongenital protrusion Inferred relationship Some 6
    Congenital sacral meningocele Associated morphology False kongenital protrusion Inferred relationship Some 1
    Congenital sacral meningocele with conotruncal heart defect syndrome (disorder) Associated morphology False kongenital protrusion Inferred relationship Some 4
    Congenital sacral meningocele with conotruncal heart defect syndrome (disorder) Associated morphology False kongenital protrusion Inferred relationship Some 5
    Myelomeningocele co-occurrent with hydrocephalus (disorder) Associated morphology False kongenital protrusion Inferred relationship Some 7
    Repair of lipomeningocele (procedure) Direct morphology False kongenital protrusion Inferred relationship Some 2
    Familial omphalocele syndrome with facial dysmorphism (disorder) Associated morphology False kongenital protrusion Inferred relationship Some 1
    Retinal detachment and occipital encephalocele Associated morphology False kongenital protrusion Inferred relationship Some 3
    Congenital sacral meningocele with conotruncal heart defect syndrome (disorder) Associated morphology False kongenital protrusion Inferred relationship Some 3
    Nasal encephalocele Associated morphology False kongenital protrusion Inferred relationship Some 1
    Capra DeMarco syndrome (disorder) Associated morphology False kongenital protrusion Inferred relationship Some 3
    Congenital cerebral meningocele Associated morphology False kongenital protrusion Inferred relationship Some 2
    Nasofrontal encephalocele Associated morphology False kongenital protrusion Inferred relationship Some 1
    Nasopharyngeal encephalocele Associated morphology False kongenital protrusion Inferred relationship Some 1
    Zechi Ceide syndrome Associated morphology False kongenital protrusion Inferred relationship Some 2
    Lethal occipital encephalocele, skeletal dysplasia syndrome (disorder) Associated morphology False kongenital protrusion Inferred relationship Some 4

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    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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