Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Is a | Connective tissue hereditary disorder | true | Inferred relationship | Some | ||
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Is a | Vitreoretinal degeneration (disorder) | true | Inferred relationship | Some | ||
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Some | ||
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Is a | Occipital encephalocele | true | Inferred relationship | Some | ||
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Occurrence | Congenital | false | Inferred relationship | Some | 10 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | anomalie du développement | false | Inferred relationship | Some | 10 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Brain structure | false | Inferred relationship | Some | 10 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | dégénérescence | false | Inferred relationship | Some | 6 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Composite structure of hyaluronic acid gel within a stromal network of collagen fibrils | false | Inferred relationship | Some | 6 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | Congenital protrusion | false | Inferred relationship | Some | 7 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Occipital lobe structure | false | Inferred relationship | Some | 7 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | Congenital failure of fusion with herniated tissue | false | Inferred relationship | Some | 8 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Bone structure of cranium | false | Inferred relationship | Some | 8 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | Atrophy | true | Inferred relationship | Some | 9 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Peripheral retina | true | Inferred relationship | Some | 9 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Occurrence | Congenital | false | Inferred relationship | Some | 11 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | anomalie du développement | false | Inferred relationship | Some | 11 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Bone structure of head | false | Inferred relationship | Some | 11 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Occipital lobe structure | false | Inferred relationship | Some | 3 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 5 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | Congenital protrusion | false | Inferred relationship | Some | 3 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 4 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Occurrence | Congenital | true | Inferred relationship | Some | 4 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | Morphologically abnormal structure | false | Inferred relationship | Some | 4 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | Congenital failure of fusion with herniated tissue | false | Inferred relationship | Some | 5 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Bone structure of cranium | false | Inferred relationship | Some | 5 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Occipital lobe structure | false | Inferred relationship | Some | 4 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Bone structure of head | false | Inferred relationship | Some | 4 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | Herniated structure (morphologic abnormality) | false | Inferred relationship | Some | 4 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | Developmental failure of fusion (morphologic abnormality) | true | Inferred relationship | Some | 3 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Bone structure of cranium | true | Inferred relationship | Some | 3 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Is a | Degenerative disorder of macula (disorder) | true | Inferred relationship | Some | ||
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Composite structure of hyaluronic acid gel within a stromal network of collagen fibrils | true | Inferred relationship | Some | 5 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Macula lutea structure | true | Inferred relationship | Some | 1 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | Atrophy | true | Inferred relationship | Some | 5 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Is a | Musculoskeletal and connective tissue disorder (disorder) | true | Inferred relationship | Some | ||
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | Herniated structure (morphologic abnormality) | false | Inferred relationship | Some | 3 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Brain structure | false | Inferred relationship | Some | 3 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | Developmental failure of fusion (morphologic abnormality) | true | Inferred relationship | Some | 4 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Structure of occipitomastoid suture of skull | true | Inferred relationship | Some | 4 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Occurrence | Congenital | true | Inferred relationship | Some | 6 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Finding site | Brain structure | true | Inferred relationship | Some | 6 | |
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. | Associated morphology | Herniated structure (morphologic abnormality) | true | Inferred relationship | Some | 6 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)