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783697000: X-linked spastic paraplegia type 16 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3759761011 X-linked spastic paraplegia type 16 (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3759762016 X-linked spastic paraplegia type 16 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3759491017 A complex hereditary spastic paraplegia with characteristics of delayed motor development, spasticity and inability to walk, later progressing to quadriplegia, motor aphasia, bowel and bladder dysfunction. Patients also present with vision problems and mild intellectual disability. The disease affects only males. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3759761011 X-linked spastic paraplegia type 16 (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3759762016 X-linked spastic paraplegia type 16 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3759491017 A complex hereditary spastic paraplegia with characteristics of delayed motor development, spasticity and inability to walk, later progressing to quadriplegia, motor aphasia, bowel and bladder dysfunction. Patients also present with vision problems and mild intellectual disability. The disease affects only males. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3426951001000118 Spastische Paraplegie, X-chromosomale, Typ 16 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3426951001000118 Spastische Paraplegie, X-chromosomale, Typ 16 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked spastic paraplegia type 16 (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked spastic paraplegia type 16 (disorder) Is a Complicated hereditary spastic paraplegia (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
X-linked spastic paraplegia type 16 (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked spastic paraplegia type 16 (disorder) Is a X-linked hereditary spastic paraplegia (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
X-linked spastic paraplegia type 16 (disorder) Finding site Spinal cord structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked spastic paraplegia type 16 (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked spastic paraplegia type 16 (disorder) Finding site Lower limb structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked spastic paraplegia type 16 (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked spastic paraplegia type 16 (disorder) Is a X-linked complex hereditary spastic paraplegia true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked spastic paraplegia type 16 (disorder) Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked spastic paraplegia type 16 (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 3
X-linked spastic paraplegia type 16 (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked spastic paraplegia type 16 (disorder) Finding site Structure of left lower limb (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 4
X-linked spastic paraplegia type 16 (disorder) Finding site Structure of right lower limb (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 5
X-linked spastic paraplegia type 16 (disorder) Interprets Movement observable true Inferred relationship Existential restriction modifier (core metadata concept) 6
X-linked spastic paraplegia type 16 (disorder) Has interpretation Absent true Inferred relationship Existential restriction modifier (core metadata concept) 6

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

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