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763351003: Spectrin-associated autosomal recessive cerebellar ataxia (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
3638655016 Spectrin-associated autosomal recessive cerebellar ataxia en Synonym Active Entire term case insensitive SNOMED CT core module
3638656015 Autosomal recessive spinocerebellar ataxia type 14 en Synonym Active Entire term case insensitive SNOMED CT core module
3638657012 Autosomal recessive cerebellar ataxia, cognitive defect syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3638658019 Spectrin-associated autosomal recessive cerebellar ataxia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3638659010 Spectrin-associated autosomal recessive cerebellar ataxia type 1 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
Spectrin-associated autosomal recessive cerebellar ataxia Is a Congenital disease true Inferred relationship Existential restriction modifier
Spectrin-associated autosomal recessive cerebellar ataxia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Spectrin-associated autosomal recessive cerebellar ataxia Is a Early onset cerebellar ataxia true Inferred relationship Existential restriction modifier
Spectrin-associated autosomal recessive cerebellar ataxia Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Spectrin-associated autosomal recessive cerebellar ataxia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Spectrin-associated autosomal recessive cerebellar ataxia Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 1
Spectrin-associated autosomal recessive cerebellar ataxia Is a Hereditary ataxia 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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