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40265002: Structure of arch of vertebra (body structure)


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
63636010 Arch of vertebra en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
492510013 Structure of arch of vertebra en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
776875015 Structure of arch of vertebra (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


198 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Structure of arch of vertebra Is a Vertebral part false Inferred relationship Some
Structure of arch of vertebra partie de Entire bone of vertebra (body structure) false Additional relationship Some
Structure of arch of vertebra Is a Posterior vertebral element true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
hydromyéloméningocèle Finding site False Structure of arch of vertebra Inferred relationship Some 6
Rachischisis is a neural tube defect, which occurs when the neural folds do not join at the midline and the undifferentiated neuroectoderm remains exposed. Rachischisis totalis (holorachischisis) is the extreme form in which the entire spinal cord remains open. Finding site False Structure of arch of vertebra Inferred relationship Some 1
Lumbar spina bifida with hydrocephalus Finding site False Structure of arch of vertebra Inferred relationship Some 3
Lumbar spina bifida with hydrocephalus - open Finding site False Structure of arch of vertebra Inferred relationship Some 3
Spina bifida with hydrocephalus - closed Finding site False Structure of arch of vertebra Inferred relationship Some 3
Spina bifida with hydrocephalus of late onset Finding site False Structure of arch of vertebra Inferred relationship Some 1
Spina bifida with stenosis of aqueduct of Sylvius Finding site False Structure of arch of vertebra Inferred relationship Some 1
A rare closed neural tube defect characterized by cystic dilatation of the central canal of the spinal cord, herniating through a posterior vertebral arch defect (spina bifida) into an expanded cerebrospinal fluid (CSF) filled dural sac (meningocele). It can be located at the caudal part of the spinal cord (terminal myelocystocele) or above conus (non-terminal myelocystocele). Finding site True Structure of arch of vertebra Inferred relationship Some 1
Cervical myelocystocele Finding site False Structure of arch of vertebra Inferred relationship Some 1
Thoracic myelocystocele Finding site False Structure of arch of vertebra Inferred relationship Some 1
Lumbar myelocystocele Finding site False Structure of arch of vertebra Inferred relationship Some 1
Lumbar spina bifida without hydrocephalus - open Finding site False Structure of arch of vertebra Inferred relationship Some 1
Sacral spina bifida without hydrocephalus - open Finding site False Structure of arch of vertebra Inferred relationship Some 1
Spina bifida without hydrocephalus - closed Finding site True Structure of arch of vertebra Inferred relationship Some 1
Thoracolumbar spina bifida without hydrocephalus - closed Finding site False Structure of arch of vertebra Inferred relationship Some 1
Fissured spine Finding site False Structure of arch of vertebra Inferred relationship Some 1
Rachischisis with hydrocephalus Finding site False Structure of arch of vertebra Inferred relationship Some 1
Myelocele with hydrocephalus (disorder) Finding site True Structure of arch of vertebra Inferred relationship Some 2
Hydromyelocele with hydrocephalus Finding site False Structure of arch of vertebra Inferred relationship Some 1
Fissured spine with hydrocephalus Finding site False Structure of arch of vertebra Inferred relationship Some 3
Closed spina bifida with Arnold-Chiari malformation Finding site True Structure of arch of vertebra Inferred relationship Some 1
Thoracolumbar spina bifida with hydrocephalus - closed (disorder) Finding site False Structure of arch of vertebra Inferred relationship Some 2
Hemimyelocele Finding site True Structure of arch of vertebra Inferred relationship Some 1
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. Finding site False Structure of arch of vertebra Inferred relationship Some 2
Spina bifida with hydrocephalus - open Finding site True Structure of arch of vertebra Inferred relationship Some 3
Spina bifida without hydrocephalus - open Finding site True Structure of arch of vertebra Inferred relationship Some 1
Myelomeningocele without hydrocephalus (disorder) Finding site True Structure of arch of vertebra Inferred relationship Some 1
Lipomyelomeningocele Finding site False Structure of arch of vertebra Inferred relationship Some 1
Occult spinal dysraphism sequence Finding site False Structure of arch of vertebra Inferred relationship Some 3
Czeizel-Losonci syndrome (CLS) is an exceedingly rare, severe, congenital genetic malformation disorder characterized by split hand/split foot, hydronephrosis, and spina bifida. Spinal and skeletal manifestations were thoracolumbar scoliosis, spina bifida (spina bifida occulta or spina bifida cystic), Bochdalek diaphragmatic hernia, and radial defects. There have been no further descriptions in the literature since 1987. Finding site False Structure of arch of vertebra Inferred relationship Some 9
Myelomeningocele co-occurrent with hydrocephalus (disorder) Finding site False Structure of arch of vertebra Inferred relationship Some 8
Occult spinal dysraphism sequence Finding site True Structure of arch of vertebra Inferred relationship Some 1
Primary tethered cord syndrome is a genetic, non-syndromic congenital malformation of the neurenteric canal, spinal cord and column characterized by progressive neurologic deterioration (pain, sensorimotor deficits, abnormal gait, decreased tone or abnormal reflexes), musculoskeletal changes (foot deformities and asymmetry, muscle atrophy, limb weakness and numbness, gait disturbances, scoliosis) and/or genitourinary manifestations (bladder and bowel dysfunction). Midline cutaneous stigmata in the lumbosacral region, such as tufts of hair, skin appendages, dimples, subcutaneous lipomas, skin discoloration or hemangiomas, are frequently associated. Finding site True Structure of arch of vertebra Inferred relationship Some 4
Spina bifida of sacral region (disorder) Finding site False Structure of arch of vertebra Inferred relationship Some 1
Spina bifida of cervical region Finding site False Structure of arch of vertebra Inferred relationship Some 2
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. Finding site True Structure of arch of vertebra Inferred relationship Some 1
Spina bifida with stenosis of aqueduct of Sylvius Finding site True Structure of arch of vertebra Inferred relationship Some 2
Spina bifida with hydrocephalus of late onset Finding site True Structure of arch of vertebra Inferred relationship Some 3
Spina bifida of dorsal region (disorder) Finding site False Structure of arch of vertebra Inferred relationship Some 2
Myelomeningocele co-occurrent with hydrocephalus (disorder) Finding site True Structure of arch of vertebra Inferred relationship Some 2
Thoracic spina bifida without hydrocephalus - open Finding site False Structure of arch of vertebra Inferred relationship Some 3
Thoracic spina bifida with hydrocephalus - open Finding site False Structure of arch of vertebra Inferred relationship Some 3
Thoracic spina bifida with hydrocephalus Finding site False Structure of arch of vertebra Inferred relationship Some 3
Lumbar spina bifida without hydrocephalus - closed Finding site False Structure of arch of vertebra Inferred relationship Some 3
Czeizel-Losonci syndrome (CLS) is an exceedingly rare, severe, congenital genetic malformation disorder characterized by split hand/split foot, hydronephrosis, and spina bifida. Spinal and skeletal manifestations were thoracolumbar scoliosis, spina bifida (spina bifida occulta or spina bifida cystic), Bochdalek diaphragmatic hernia, and radial defects. There have been no further descriptions in the literature since 1987. Finding site True Structure of arch of vertebra Inferred relationship Some 3
Thoracic spina bifida without hydrocephalus - closed Finding site False Structure of arch of vertebra Inferred relationship Some 3
Rachischisis with hydrocephalus Finding site True Structure of arch of vertebra Inferred relationship Some 3
Cervical spina bifida without hydrocephalus - open Finding site False Structure of arch of vertebra Inferred relationship Some 3
Cervical spina bifida without hydrocephalus - closed Finding site False Structure of arch of vertebra Inferred relationship Some 3
Spina bifida aperta of cervical spine (disorder) Finding site False Structure of arch of vertebra Inferred relationship Some 4
Spina bifida with hydrocephalus - closed Finding site True Structure of arch of vertebra Inferred relationship Some 2
Fissured spine with hydrocephalus Finding site False Structure of arch of vertebra Inferred relationship Some 2
Lumbar spina bifida with hydrocephalus - open Finding site False Structure of arch of vertebra Inferred relationship Some 5
Sacral spina bifida without hydrocephalus - closed Finding site False Structure of arch of vertebra Inferred relationship Some 2
Dandy-Walker syndrome with spina bifida Finding site True Structure of arch of vertebra Inferred relationship Some 5
hydromyéloméningocèle Finding site False Structure of arch of vertebra Inferred relationship Some 2
Split spinal cord malformation (disorder) Finding site True Structure of arch of vertebra Inferred relationship Some 3
Congenital spinal meningocele Finding site True Structure of arch of vertebra Inferred relationship Some 1
Meningomyelocele of lumbosacral spine (disorder) Finding site False Structure of arch of vertebra Inferred relationship Some 2
Lipomyelomeningocele Finding site False Structure of arch of vertebra Inferred relationship Some 2
Congenital spinal hydromeningocele Finding site False Structure of arch of vertebra Inferred relationship Some 3
Meningomyelocele (disorder) Finding site True Structure of arch of vertebra Inferred relationship Some 1
Fetal spina bifida (disorder) Finding site True Structure of arch of vertebra Inferred relationship Some 1
Faun tail syndrome Finding site True Structure of arch of vertebra Inferred relationship Some 3
hydromyélocèle Finding site False Structure of arch of vertebra Inferred relationship Some 2
Structure of fetal arch of vertebra (body structure) Is a True Structure of arch of vertebra Inferred relationship Some
Rachischisis is a neural tube defect, which occurs when the neural folds do not join at the midline and the undifferentiated neuroectoderm remains exposed. Rachischisis totalis (holorachischisis) is the extreme form in which the entire spinal cord remains open. Finding site True Structure of arch of vertebra Inferred relationship Some 4
Rachischisis is a neural tube defect, which occurs when the neural folds do not join at the midline and the undifferentiated neuroectoderm remains exposed. Rachischisis partialis (merorachischisis) is the partial form where the spinal cord is partially closed and partially open. Finding site True Structure of arch of vertebra Inferred relationship Some 1
A rare subtype of split cord malformation characterised by each hemicord contained in its own dural sac, typically with an intervening bony septum. Finding site True Structure of arch of vertebra Inferred relationship Some 1
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. Finding site True Structure of arch of vertebra Inferred relationship Some 1
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. Finding site True Structure of arch of vertebra Inferred relationship Some 1
A rare, closed spinal dysraphism with characteristics of a myelocystocele at the termination of the spinal cord. It may be an isolated anomaly or be associated with other defects, including sacral agenesis, anorectal and genitourinary anomalies. The conus is not identifiable. The myelocystocele sac may have a significant lipomatous component (terminal lipomyelocystocele). Finding site True Structure of arch of vertebra Inferred relationship Some 2
A rare closed spinal dysraphism with characteristics of myelocystocele located above the conus region. Also considered as a form of saccular limited dorsal myeloschisis. Finding site True Structure of arch of vertebra Inferred relationship Some 2

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