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783764008: Autosomal recessive spastic paraplegia type 56 (disorder)


Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3760261015 Autosomal recessive spastic paraplegia type 56 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3760262010 Autosomal recessive spastic paraplegia type 56 en Synonym Active Case insensitive SNOMED CT core
3760241014 A rare form of hereditary spastic paraplegia with characteristics of delayed walking, toe walking, unsteady and spastic gait, hyperreflexia of the lower limbs, and extensor plantar responses. Upper limbs spasticity and dystonia, subclinical axonal neuropathy, cognitive impairment and intellectual disability have also been associated. Caused by homozygous or compound heterozygous mutation in the CYP2U1 gene on chromosome 4q25. 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 56 Occurrence Congenital false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 56 Finding site Spinal cord structure true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 56 Is a Hereditary spastic paraplegia false Inferred relationship Some
Autosomal recessive spastic paraplegia type 56 Associated morphology Degeneration false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 56 Is a Autosomal recessive hereditary disorder false Inferred relationship Some
Autosomal recessive spastic paraplegia type 56 Finding site Structure of lower limb false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 56 Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 56 Is a Autosomal recessive hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 56 Clinical course Progressive true Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 56 Interprets Movement true Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 56 Finding site Structure of right lower limb true Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 56 Finding site Structure of left lower limb true Inferred relationship Some 5
Autosomal recessive spastic paraplegia type 56 Interprets Movement observable true Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 56 Has interpretation Absent true Inferred relationship Some 4

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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