Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4591650014 | A rare, neural tube defect characterized by localized longitudinal division of the spinal cord with an interposed osseous, cartilaginous or fibrous septum and double dural sac, typically occurring at the thoracic or lumbar level. Local vertebral segmental defects, syringomyelia, meningocele and intraspinal tumors may be associated. Variable clinical presentation includes pain, scoliosis, asymmetry and weakness of the lower limbs, neurological deficits, sphincter dysfunction, and various cutaneous abnormalities overlying the spine, such as hypertrichosis, dimple, hemangioma, subcutaneous mass or pigmented nevus. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4591652018 | A rare, neural tube defect characterised by localised longitudinal division of the spinal cord with an interposed osseous, cartilaginous or fibrous septum and double dural sac, typically occurring at the thoracic or lumbar level. Local vertebral segmental defects, syringomyelia, meningocele and intraspinal tumours may be associated. Variable clinical presentation includes pain, scoliosis, asymmetry and weakness of the lower limbs, neurological deficits, sphincter dysfunction, and various cutaneous abnormalities overlying the spine, such as hypertrichosis, dimple, haemangioma, subcutaneous mass or pigmented naevus. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5399274018 | A rare subtype of split cord malformation characterized by each hemicord contained in its own dural sac, typically with an intervening bony septum. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5399275017 | A rare subtype of split cord malformation characterised by each hemicord contained in its own dural sac, typically with an intervening bony septum. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4591647011 | Split spinal cord malformation type 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4591648018 | Split spinal cord malformation type I (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 4591649014 | Split spinal cord malformation type I | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| A rare subtype of split cord malformation characterised by each hemicord contained in its own dural sac, typically with an intervening bony septum. | Is a | Split spinal cord malformation (disorder) | true | Inferred relationship | Some | ||
| A rare subtype of split cord malformation characterised by each hemicord contained in its own dural sac, typically with an intervening bony septum. | Occurrence | Congenital | true | 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 | Structure of arch of vertebra | true | 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. | Associated morphology | Developmental failure of fusion (morphologic abnormality) | true | 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. | Pathological process (attribute) | Pathological developmental process | true | 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. | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| 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 | Neural tube structure | true | Inferred relationship | Some | 2 | |
| A rare subtype of split cord malformation characterised by each hemicord contained in its own dural sac, typically with an intervening bony septum. | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 2 | |
| A rare subtype of split cord malformation characterised by each hemicord contained in its own dural sac, typically with an intervening bony septum. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
| A rare subtype of split cord malformation characterised by each hemicord contained in its own dural sac, typically with an intervening bony septum. | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
| 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 | Spinal cord structure | true | Inferred relationship | Some | 3 | |
| A rare subtype of split cord malformation characterised by each hemicord contained in its own dural sac, typically with an intervening bony septum. | Associated morphology | Congenital septation | true | Inferred relationship | Some | 3 | |
| A rare subtype of split cord malformation characterised by each hemicord contained in its own dural sac, typically with an intervening bony septum. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR