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716998009: Joubert syndrome with ocular defect (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
3308130019 Joubert syndrome with ocular defect (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308131015 Joubert syndrome with ocular defect en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308132010 Joubert syndrome with retinopathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401440019 Joubert syndrome with ocular defect is, along with pure JS, the most frequent subtype of Joubert syndrome and related disorders characterized by the neurological features of JS associated with retinal dystrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401441015 Joubert syndrome with ocular defect is, along with pure JS, the most frequent subtype of Joubert syndrome and related disorders characterised by the neurological features of JS associated with retinal dystrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308130019 Joubert syndrome with ocular defect (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308131015 Joubert syndrome with ocular defect en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308132010 Joubert syndrome with retinopathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308133017 The most frequent subtype of Joubert syndrome with manifestation of neurological features of Joubert Syndrome associated with retinal dystrophy. Prevalence is unknown. Age of onset and severity of retinal involvement are variable, ranging from congenital to progressive retinopathy with partial conservation of vision. To date, the most frequently mutated gene in this subtype is AHI1 (6q23.2), which accounts for about 20% of cases, following autosomal recessive inheritance. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401440019 Joubert syndrome with ocular defect is, along with pure JS, the most frequent subtype of Joubert syndrome and related disorders characterized by the neurological features of JS associated with retinal dystrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401441015 Joubert syndrome with ocular defect is, along with pure JS, the most frequent subtype of Joubert syndrome and related disorders characterised by the neurological features of JS associated with retinal dystrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
523811000274114 Joubert-Syndrom mit Retinopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3419371001000113 Joubert-Syndrom mit Augendefekt de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
895361000172116 syndrome de Joubert avec anomalie oculaire fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
985301000172111 JS-O - Joubert syndrome with ocular defect fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
895361000172116 syndrome de Joubert avec anomalie oculaire fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
985301000172111 JS-O - Joubert syndrome with ocular defect fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
523811000274114 Joubert-Syndrom mit Retinopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3419371001000113 Joubert-Syndrom mit Augendefekt 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
Joubert syndrome with ocular defect Is a Retinal disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Joubert syndrome with ocular defect Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Joubert syndrome with ocular defect Is a Joubert syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Joubert syndrome with ocular defect Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Joubert syndrome with ocular defect Associated morphology Aplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Joubert syndrome with ocular defect Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Joubert syndrome with ocular defect Finding site Cerebellar vermis structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Joubert syndrome with ocular defect Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Joubert syndrome with ocular defect Associated morphology Aplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Joubert syndrome with ocular defect Finding site Cerebellar vermis structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Joubert syndrome with ocular defect Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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