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784343003: Autosomal recessive spastic ataxia with leukoencephalopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3763695011 ARSAL - autosomal recessive spastic ataxia with leukoencephalopathy en Synonym Active Entire term case sensitive SNOMED CT core module
3763696012 Autosomal recessive spastic ataxia with leukoencephalopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3763697015 Autosomal recessive spastic ataxia type 3 en Synonym Active Entire term case insensitive SNOMED CT core module
3763698013 Autosomal recessive spastic ataxia with leukoencephalopathy en Synonym Active Entire term case insensitive SNOMED CT core module
3763699017 SPAX3 - autosomal recessive spastic ataxia type 3 en Synonym Active Entire term case sensitive SNOMED CT core module
3789567015 Autosomal recessive spastic ataxia with leucoencephalopathy en Synonym Active Entire term case insensitive SNOMED CT core module
3789568013 ARSAL - autosomal recessive spastic ataxia with leucoencephalopathy 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 spastic ataxia with leukoencephalopathy Is a Hereditary ataxia true Inferred relationship Existential restriction modifier
Autosomal recessive spastic ataxia with leukoencephalopathy Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal recessive spastic ataxia with leukoencephalopathy Is a Leukoencephalopathy true Inferred relationship Existential restriction modifier
Autosomal recessive spastic ataxia with leukoencephalopathy Is a Cerebellar ataxia true Inferred relationship Existential restriction modifier
Autosomal recessive spastic ataxia with leukoencephalopathy Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Autosomal recessive spastic ataxia with leukoencephalopathy Finding site Cerebral white matter structure true Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic ataxia with leukoencephalopathy Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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