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278509004: Congenital non-progressive ataxia (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
415440014 Congenital non-progressive ataxia en Synonym Active Entire term case insensitive SNOMED CT core module
671675015 Congenital non-progressive ataxia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital non-progressive ataxia Is a Cerebral palsy false Inferred relationship Existential restriction modifier
Congenital non-progressive ataxia Is a Congenital anomaly of nervous system false Inferred relationship Existential restriction modifier
Congenital non-progressive ataxia Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier
Congenital non-progressive ataxia Finding site Structure of cerebrum false Inferred relationship Existential restriction modifier
Congenital non-progressive ataxia Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital non-progressive ataxia Is a Ataxia true Inferred relationship Existential restriction modifier
Congenital non-progressive ataxia Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital non-progressive ataxia Finding site Structure of nervous system false Inferred relationship Existential restriction modifier 1
Congenital non-progressive ataxia Is a Finding of lesion false Inferred relationship Existential restriction modifier
Congenital non-progressive ataxia Finding site Structure of nervous system false Inferred relationship Existential restriction modifier 1
Congenital non-progressive ataxia Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital non-progressive ataxia Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Congenital non-progressive ataxia Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Congenital non-progressive ataxia Finding site Structure of nervous system false Inferred relationship Existential restriction modifier 2
Congenital non-progressive ataxia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital non-progressive ataxia Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
Congenital non-progressive ataxia Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 1
Congenital non-progressive ataxia Clinical course Non-progressive true Inferred relationship Existential restriction modifier 2
Congenital non-progressive ataxia Is a Congenital disease true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal recessive cerebelloparenchymal disorder type 3 Is a True Congenital non-progressive ataxia Inferred relationship Existential restriction modifier
X-linked non progressive cerebellar ataxia Is a True Congenital non-progressive ataxia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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