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715436007: Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3302596011 Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302599016 Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302623015 Cerebellar hypoplasia and tapetoretinal degeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302596011 Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3302596011 Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302599016 Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3302599016 Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302623015 Cerebellar hypoplasia and tapetoretinal degeneration en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3302623015 Cerebellar hypoplasia and tapetoretinal degeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3429411001000118 Zerebelläre Hypoplasie-tapetoretinale Degeneration-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5835471000241118 hypoplasie congénitale du cervelet concomitante d'un dégénérescence tapétorétinienne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5835481000241116 hypoplasie cérébelleuse congénitale concomitante d'une dégénérescence tapétorétinienne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5835471000241118 hypoplasie congénitale du cervelet concomitante d'un dégénérescence tapétorétinienne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5835481000241116 hypoplasie cérébelleuse congénitale concomitante d'une dégénérescence tapétorétinienne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3429411001000118 Zerebelläre Hypoplasie-tapetoretinale Degeneration-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) Is a Congenital cerebellar hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) Finding site The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) Finding site Cerebellar structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) Finding site The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) Finding site Cerebellar structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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