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723822009: Autosomal recessive spastic paraplegia type 46 (disorder)


Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3426268013 Autosomal recessive spastic paraplegia type 46 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3426269017 Autosomal recessive spastic paraplegia type 46 en Synonym Active Case insensitive SNOMED CT core
3426270016 A rare complex type of hereditary spastic paraplegia with onset, in infancy or childhood of the typical signs of spastic paraplegia (i.e. spastic gait and weakness of the lower limbs) associated with a variety of additional manifestations including upper limb spasticity and weakness, pseudobulbar dysarthria, bladder dysfunction, cerebellar ataxia, cataracts, and cognitive impairment that can progress to dementia. Brain imaging may show thinning of the corpus callosum and mild atrophy of the cerebrum and cerebellum. Caused by mutations in the GBA2 gene (9p13.2) encoding non-lysosomal glucosylceramidase. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive spastic paraplegia type 46 Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 46 Is a Autosomal recessive hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 46 Clinical course Progressive true Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 46 Interprets Movement true Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 46 Finding site Structure of right lower limb true Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 46 Finding site Structure of left lower limb true Inferred relationship Some 5
Autosomal recessive spastic paraplegia type 46 Interprets Movement observable true Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 46 Has interpretation Absent true Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 46 Is a Autosomal recessive hereditary disorder false Inferred relationship Some
Autosomal recessive spastic paraplegia type 46 Is a Complicated hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 46 Occurrence Congenital false Inferred relationship Some
Autosomal recessive spastic paraplegia type 46 Finding site Structure of lower limb false Inferred relationship Some
Autosomal recessive spastic paraplegia type 46 Associated morphology Degeneration false Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 46 Finding site Spinal cord structure false Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 46 Finding site Cerebellar structure false Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 46 Associated morphology Degeneration false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 46 Occurrence Congenital false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 46 Finding site Spinal cord structure true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 46 Occurrence Congenital false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 46 Finding site Structure of lower limb 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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