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763367009: Autosomal recessive spastic paraplegia type 48 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3640234010 Autosomal recessive spastic paraplegia type 48 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3640235011 Autosomal recessive spastic paraplegia type 48 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3640236012 A form of hereditary spastic paraplegia with usual characteristics of a pure phenotype of a slowly progressive spastic paraplegia associated with urinary incontinence with an onset in mid to late-adulthood. A complex phenotype, with the additional findings of cognitive impairment, sensorimotor polyneuropathy, ataxia and Parkinsonism as well as thin corpus callosum and white matter lesions (seen on magnetic resonance imaging) has also been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
922771000172116 SPG48 - spastic paraplegia type 48 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
977291000172112 paraplégie spastique autosomique récessive type 48 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
887591000172113 autosomaal recessieve spastische paraplegie type 48 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
948491000172114 SPG48 - spastische paraplegie type 48 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive spastic paraplegia type 48 (disorder) Is a Hereditary spastic paraplegia false Inferred relationship Some
Autosomal recessive spastic paraplegia type 48 (disorder) Is a Autosomal recessive hereditary disorder false Inferred relationship Some
Autosomal recessive spastic paraplegia type 48 (disorder) Occurrence Congenital false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 48 (disorder) Finding site Lower limb structure (body structure) false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 48 (disorder) Occurrence Congenital false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 48 (disorder) Finding site Spinal cord structure true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 48 (disorder) Associated morphology Degeneration false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 48 (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 48 (disorder) Is a Autosomal recessive hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 48 (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 48 (disorder) Finding site Lower limb structure (body structure) false Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 48 (disorder) Interprets Movement true Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 48 (disorder) Finding site Structure of right lower limb (body structure) true Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 48 (disorder) Finding site Structure of left lower limb (body structure) true Inferred relationship Some 5
Autosomal recessive spastic paraplegia type 48 (disorder) Interprets Movement observable true Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 48 (disorder) Has interpretation Absent true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Belgian subset for medical problems in patient health records

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