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764686003: Autosomal recessive spastic paraplegia type 15 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3654867016 Spastic paraplegia, retinal degeneration syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3654869018 Kjellin syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3654870017 Autosomal recessive spastic paraplegia type 15 en Synonym Active Entire term case insensitive SNOMED CT core module
3654871018 Hereditary spastic paraparesis type 15 en Synonym Active Entire term case insensitive SNOMED CT core module
3654872013 Autosomal recessive spastic paraplegia type 15 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive spastic paraplegia type 15 Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 15 Is a Complicated hereditary spastic paraplegia true Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 15 Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 15 Finding site Lower limb structure false Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 15 Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 15 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 15 Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 15 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 15 Is a Autosomal recessive hereditary spastic paraplegia true Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 15 Clinical course Progressive true Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 15 Interprets Movement true Inferred relationship Existential restriction modifier 6
Autosomal recessive spastic paraplegia type 15 Finding site Structure of right lower limb true Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 15 Finding site Structure of left lower limb true Inferred relationship Existential restriction modifier 5
Autosomal recessive spastic paraplegia type 15 Interprets Movement observable true Inferred relationship Existential restriction modifier 4
Autosomal recessive spastic paraplegia type 15 Has interpretation Absent true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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