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1259038005: complexe autosomaal dominante hereditaire spastische paraplegie (aandoening)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
5155527013 Autosomal dominant complex hereditary spastic paraplegia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
14114871000146113 complexe autosomaal dominante hereditaire spastische paraplegie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14114881000146110 complexe autosomaal dominante HSP nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14114891000146112 complexe autosomaal dominante hereditaire spastische paraplegie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


10 descendants. Search Descendants:

Expanded Value Set


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

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

This concept is not in any reference sets

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