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716998009: Joubert syndrome with ocular defect (disorder)


Status: current, Primitive. 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 Case sensitive SNOMED CT core
3308131015 Joubert syndrome with ocular defect en Synonym Active Case sensitive SNOMED CT core
3308132010 Joubert syndrome with retinopathy en Synonym Active Case sensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Joubert syndrome with ocular defect Pathological process Pathological developmental process true Inferred relationship Some 1
Joubert syndrome with ocular defect Associated morphology Aplasia true Inferred relationship Some 1
Joubert syndrome with ocular defect Finding site Cerebellar vermis structure true Inferred relationship Some 1
Joubert syndrome with ocular defect Occurrence Congenital true Inferred relationship Some 1
Joubert syndrome with ocular defect Is a Retinal disorder true Inferred relationship Some
Joubert syndrome with ocular defect Is a Hereditary disorder of the visual system true Inferred relationship Some
Joubert syndrome with ocular defect Is a Joubert syndrome true Inferred relationship Some
Joubert syndrome with ocular defect Finding site Retinal structure true Inferred relationship Some 2
Joubert syndrome with ocular defect Associated morphology Aplasia false Inferred relationship Some 2
Joubert syndrome with ocular defect Occurrence Congenital false Inferred relationship Some 2
Joubert syndrome with ocular defect Finding site Cerebellar vermis structure false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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