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715369006: Autosomal recessive cerebelloparenchymal disorder type 3 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3302378015 Autosomal recessive cerebelloparenchymal disorder type 3 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3302379011 Autosomal recessive cerebelloparenchymal disorder type 3 en Synonym Active Entire term case insensitive SNOMED CT core module
3302380014 Cerebelloparenchymal disorder III en Synonym Active Only initial character case insensitive SNOMED CT core module
3303324010 SCAR2 (spinocerebellar ataxia autosomal recessive 2) 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
Autosomal recessive cerebelloparenchymal disorder type 3 Is a Hereditary cerebellar degeneration false Inferred relationship Existential restriction modifier
Autosomal recessive cerebelloparenchymal disorder type 3 Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal recessive cerebelloparenchymal disorder type 3 Is a Spinocerebellar ataxia true Inferred relationship Existential restriction modifier
Autosomal recessive cerebelloparenchymal disorder type 3 Is a Dysgenesis of the cerebellum true Inferred relationship Existential restriction modifier
Autosomal recessive cerebelloparenchymal disorder type 3 Is a Congenital non-progressive ataxia true Inferred relationship Existential restriction modifier
Autosomal recessive cerebelloparenchymal disorder type 3 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 3
Autosomal recessive cerebelloparenchymal disorder type 3 Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 3
Autosomal recessive cerebelloparenchymal disorder type 3 Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 4
Autosomal recessive cerebelloparenchymal disorder type 3 Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Autosomal recessive cerebelloparenchymal disorder type 3 Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 4
Autosomal recessive cerebelloparenchymal disorder type 3 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 5
Autosomal recessive cerebelloparenchymal disorder type 3 Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 5
Autosomal recessive cerebelloparenchymal disorder type 3 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal recessive cerebelloparenchymal disorder type 3 Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive cerebelloparenchymal disorder type 3 Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive cerebelloparenchymal disorder type 3 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Autosomal recessive cerebelloparenchymal disorder type 3 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 3
Autosomal recessive cerebelloparenchymal disorder type 3 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 4
Autosomal recessive cerebelloparenchymal disorder type 3 Clinical course Non-progressive true Inferred relationship Existential restriction modifier 2
Autosomal recessive cerebelloparenchymal disorder type 3 Is a Developmental hereditary disorder 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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