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703542000: Retinal detachment and occipital encephalocele (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5449639012 A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5449640014 A rare systemic disorder characterized by vitreoretinal and macular degeneration, as well as occipital encephalocele. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3009167015 Retinal detachment and occipital encephalocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009293017 Knobloch syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3009395014 Retinal detachment and occipital encephalocoele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009400010 Retinal detachment and occipital encephalocele (disorder) 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
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 Developmental anomaly 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 Degeneration 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 Developmental anomaly 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)

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