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763402002: Spastic paraplegia, neuropathy, poikiloderma syndrome (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
3642110017 Spastic paraplegia, neuropathy, poikiloderma syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3642111018 Spastic paraplegia, neuropathy, poikiloderma syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3642277015 Antinolo Nieto Borrego syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

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

This concept is not in any reference sets

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