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1259038005: Autosomal dominant complex hereditary spastic paraplegia (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Dec 2022. Module: SNOMED CT core module

Descriptions:

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


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 Existential restriction modifier
Autosomal dominant complex hereditary spastic paraplegia Is a Autosomal dominant hereditary spastic paraplegia true Inferred relationship Existential restriction modifier
Autosomal dominant complex hereditary spastic paraplegia Clinical course Progressive true Inferred relationship Existential restriction modifier 3
Autosomal dominant complex hereditary spastic paraplegia Interprets Movement true Inferred relationship Existential restriction modifier 6
Autosomal dominant complex hereditary spastic paraplegia Finding site Structure of left lower limb true Inferred relationship Existential restriction modifier 4
Autosomal dominant complex hereditary spastic paraplegia Finding site Structure of right lower limb true Inferred relationship Existential restriction modifier 5
Autosomal dominant complex hereditary spastic paraplegia Interprets Movement observable true Inferred relationship Existential restriction modifier 2
Autosomal dominant complex hereditary spastic paraplegia Has interpretation Absent true Inferred relationship Existential restriction modifier 2
Autosomal dominant complex hereditary spastic paraplegia Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant complex hereditary spastic paraplegia Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal dominant spastic paraplegia type 17 Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Existential restriction modifier
Spastic paraplegia, neuropathy, poikiloderma syndrome Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 36 Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Existential restriction modifier
Spastic paraplegia with Paget disease of bone syndrome Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Existential restriction modifier
Spastic paraplegia with precocious puberty syndrome Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 29 Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Existential restriction modifier
Spastic paraplegia, nephritis, deafness syndrome Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 38 Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 9A Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Existential restriction modifier
Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome Is a True Autosomal dominant complex hereditary spastic paraplegia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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