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1259038005: Autosomal dominant complex hereditary spastic paraplegia (disorder)


Status: current, Defined. Date: 31-Dec 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5155526016 Autosomal dominant complex hereditary spastic paraplegia (disorder) en Fully specified name Active Case insensitive SNOMED CT core
5155527013 Autosomal dominant complex hereditary spastic paraplegia en Synonym Active Case insensitive SNOMED CT core


10 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Silver disease Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Some
Spastic paraplegia, neuropathy, poikiloderma syndrome Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Some
Autosomal dominant spastic paraplegia type 36 Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Some
Spastic paraplegia with Paget disease of bone syndrome Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Some
Spastic paraplegia with precocious puberty syndrome Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Some
Autosomal dominant spastic paraplegia type 29 Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Some
Spastic paraplegia, nephritis, deafness syndrome Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Some
Autosomal dominant spastic paraplegia type 38 Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Some
Autosomal dominant spastic paraplegia type 9A Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Some
Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Some

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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