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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

    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 Some
    Congenital failure of fusion with herniated tissue Is a Congenital protrusion false Inferred relationship Some
    Congenital failure of fusion with herniated tissue Is a Developmental failure of fusion (morphologic abnormality) false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Nasal encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Nasal encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 3
    Congenital spinal hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    Congenital spinal hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 3
    hydroméningocèle crânienne congénitale Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    hydroméningocèle crânienne congénitale Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Repair of meningoencephalocele Direct morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    Repair of meningoencephalocele Direct morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Thoracic hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    Thoracic hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Spina bifida of lumbar region Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Congenital cerebral meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    hydroméningocèle Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    [X]Encephalocele of other sites Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Cervical spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Temporal encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    Meningoencephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Congenital spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Hydrencephalomeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Frontoethmoidal encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Parietal encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    Encephalocele of orbit Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    Frontal encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Meningomyelocele/myelocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 3
    hydromyéloméningocèle Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 3
    hernie endo-auriculaire congénitale Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Congenital cerebral hernia Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    encéphalocystocèle Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Occipital encephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    Encephalocele of other specified site Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Lumbar spina bifida with hydrocephalus - closed Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Encephalocele NOS Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Encephalomyelocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Congenital sacral meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Lumbar spina bifida without hydrocephalus - closed Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Repair of encephalocele Direct morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    A rare disorder that presents as a flat neural placode (at the level of the skin of the back) that is exposed to the environment. The lack of expansion of the subarachnoid space distinguishes this lesion from myelomeningocele. Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    Encephalocystocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Cervical spinal hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Spinal meningocele of unspecified site Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 3
    Thoracic spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Lumbar spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Spinal meningocele NOS Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 3
    Myelocele NOS Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    Spinal meningocele NOS Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 3
    Spinal meningocele of unspecified site Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 3
    Myelocele of unspecified site Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    Spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Thoracic spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Thoracic myelocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 4
    Lumbar spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Cervical spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Lumbar myelocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 4
    Cervical myelocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 4
    Cervical spinal hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Encephalocele of vertex (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Known OR suspected fetal spina bifida with myelomeningocele affecting obstetrical care Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Known OR suspected fetal spina bifida with myelomeningocele affecting obstetrical care Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Encephalocele of vertex (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Myelocele with hydrocephalus (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Cervical spinal hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 4
    A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 8
    Congenital laryngocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 3
    Congenital laryngocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Congenital spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 6
    Congenital spinal hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 9
    Von Voss-Cherstvoy syndrome is a very rare disorder with phocomelia of upper limbs, encephalocele, variable brain anomalies, urogenital abnormalities, and thrombocytopenia. Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 6
    Thoracic spinal meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 3
    Spina bifida-hypospadias syndrome is a rare developmental defect during embryogenesis disorder characterized by the specific association of glandular hypospadias and lumbo-sacral spina bifida. Affected individuals may or may not present additional congenital anomalies, such as hydrocephaly, microstomia, patent ductus arteriosus, cryptorchidism, intestinal malrotation, rocker-bottom feet, and hypertrichosis. Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Spina bifida-hypospadias syndrome is a rare developmental defect during embryogenesis disorder characterized by the specific association of glandular hypospadias and lumbo-sacral spina bifida. Affected individuals may or may not present additional congenital anomalies, such as hydrocephaly, microstomia, patent ductus arteriosus, cryptorchidism, intestinal malrotation, rocker-bottom feet, and hypertrichosis. Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 5
    Encephalocystocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    Von Voss-Cherstvoy syndrome is a very rare disorder with phocomelia of upper limbs, encephalocele, variable brain anomalies, urogenital abnormalities, and thrombocytopenia. Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 3
    Encephalocele of orbit Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Congenital spinal hydromeningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 5
    Congenital cerebral meningocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by occipital atretic cephalocele associated with a specific facial dysmorphism (consisting of prominent forehead, narrow palpebral fissures, midface deficiency, narrow, malformed ears, broad nose and nasal root, grooved nasal tip and columella, laterally angulated, hypoplastic nares, short philtrum, thin upper lip, clift lip/palate, severe oligodontia, prominent chin) and large feet with sandal gap. Intellectual disability, developmental delay and hypoplastic finger and toenails have also been reported. Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 5
    Lethal occipital encephalocele-skeletal dysplasia syndrome is 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. Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 1
    Meningoencephalocele Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 2
    Myelocele with hydrocephalus (disorder) Associated morphology False Congenital failure of fusion with herniated tissue Inferred relationship Some 4

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