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723622007: X-linked spastic paraplegia type 2 (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3425300014 X-linked spastic paraplegia type 2 (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3425301013 X-linked spastic paraplegia type 2 en Synonym Active Entire term case sensitive SNOMED CT core module
3425302018 Spastic gait type 2 en Synonym Active Entire term case insensitive SNOMED CT core module
3425303011 Spastic paraparesis type 2 en Synonym Active Entire term case insensitive SNOMED CT core module
3425304017 Spastic paraplegia type 2 en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked spastic paraplegia type 2 Is a Hereditary spastic paraplegia false Inferred relationship Existential restriction modifier
X-linked spastic paraplegia type 2 Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
X-linked spastic paraplegia type 2 Is a Leukodystrophy true Inferred relationship Existential restriction modifier
X-linked spastic paraplegia type 2 Is a Inherited optic neuropathy true Inferred relationship Existential restriction modifier
X-linked spastic paraplegia type 2 Is a Hereditary disorder of the visual system false Inferred relationship Existential restriction modifier
X-linked spastic paraplegia type 2 Occurrence Congenital false Inferred relationship Existential restriction modifier 4
X-linked spastic paraplegia type 2 Finding site Optic nerve structure false Inferred relationship Existential restriction modifier 4
X-linked spastic paraplegia type 2 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 5
X-linked spastic paraplegia type 2 Finding site Spinal cord structure false Inferred relationship Existential restriction modifier 5
X-linked spastic paraplegia type 2 Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 5
X-linked spastic paraplegia type 2 Occurrence Congenital false Inferred relationship Existential restriction modifier 7
X-linked spastic paraplegia type 2 Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 6
X-linked spastic paraplegia type 2 Associated morphology Myelin sheath alteration false Inferred relationship Existential restriction modifier 6
X-linked spastic paraplegia type 2 Finding site Structure of nervous system false Inferred relationship Existential restriction modifier 6
X-linked spastic paraplegia type 2 Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 5
X-linked spastic paraplegia type 2 Finding site Lower limb structure false Inferred relationship Existential restriction modifier 7
X-linked spastic paraplegia type 2 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 1
X-linked spastic paraplegia type 2 Occurrence Congenital false Inferred relationship Existential restriction modifier 1
X-linked spastic paraplegia type 2 Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 1
X-linked spastic paraplegia type 2 Is a X-linked hereditary spastic paraplegia true Inferred relationship Existential restriction modifier
X-linked spastic paraplegia type 2 Finding site White matter structure of brain and spinal cord true Inferred relationship Existential restriction modifier 5
X-linked spastic paraplegia type 2 Associated morphology Myelin sheath alteration true Inferred relationship Existential restriction modifier 3
X-linked spastic paraplegia type 2 Finding site Myelinated nerve fiber structure true Inferred relationship Existential restriction modifier 3
X-linked spastic paraplegia type 2 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
X-linked spastic paraplegia type 2 Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier
X-linked spastic paraplegia type 2 Clinical course Progressive true Inferred relationship Existential restriction modifier 6
X-linked spastic paraplegia type 2 Finding site Optic nerve structure true Inferred relationship Existential restriction modifier 2
X-linked spastic paraplegia type 2 Finding site Lower limb structure false Inferred relationship Existential restriction modifier 4
X-linked spastic paraplegia type 2 Is a Second cranial nerve finding true Inferred relationship Existential restriction modifier
X-linked spastic paraplegia type 2 Interprets Movement true Inferred relationship Existential restriction modifier 9
X-linked spastic paraplegia type 2 Finding site Structure of right lower limb true Inferred relationship Existential restriction modifier 4
X-linked spastic paraplegia type 2 Finding site Structure of left lower limb true Inferred relationship Existential restriction modifier 8
X-linked spastic paraplegia type 2 Interprets Movement observable true Inferred relationship Existential restriction modifier 7
X-linked spastic paraplegia type 2 Has interpretation Absent true Inferred relationship Existential restriction modifier 7
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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