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1187506008: Autosomal recessive spastic paraplegia type 77 (disorder)


Status: current, Primitive. Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4674029012 Autosomal recessive spastic paraplegia type 77 en Synonym Active Case insensitive SNOMED CT core
4674030019 Autosomal recessive spastic paraplegia type 77 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4674031015 A rare pure or complex hereditary spastic paraplegia with characteristics of infancy to childhood onset of slowly progressive lower limb spasticity, delayed motor milestones, gait disturbances, hyperreflexia and various muscle abnormalities, including weakness, hypotonia, intention tremor and amyotrophy. Ocular abnormalities (e.g. strabismus, ptosis) and other neurological abnormalities, such as dysarthria, seizures and extensor plantar responses may also be associated. 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 77 Is a Autosomal recessive hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 77 Clinical course Progressive true Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 77 Finding site Structure of lower limb false Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 77 Finding site Spinal cord structure true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 77 Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 77 Interprets Movement true Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 77 Finding site Structure of right lower limb true Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 77 Finding site Structure of left lower limb true Inferred relationship Some 5
Autosomal recessive spastic paraplegia type 77 Interprets Movement observable true Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 77 Has interpretation Absent true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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