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448045004: Fragile X associated tremor ataxia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2011. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2898386017 Fragile X associated tremor ataxia syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
2900005013 Fragile X associated tremor ataxia syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
1780771000000110 FXTAS - Fragile X associated tremor ataxia syndrome en Synonym Active Entire term case sensitive SNOMED CT United Kingdom Edition module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fragile X associated tremor ataxia syndrome Is a Degenerative disorder true Inferred relationship Existential restriction modifier
Fragile X associated tremor ataxia syndrome Is a System disorder of the nervous system true Inferred relationship Existential restriction modifier
Fragile X associated tremor ataxia syndrome Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Fragile X associated tremor ataxia syndrome Finding site Structure of nervous system true Inferred relationship Existential restriction modifier 1
Fragile X associated tremor ataxia syndrome Is a Cerebellar ataxia true Inferred relationship Existential restriction modifier
Fragile X associated tremor ataxia syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
Fragile X associated tremor ataxia syndrome Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Fragile X associated tremor ataxia syndrome Is a Hereditary ataxia true Inferred relationship Existential restriction modifier
Fragile X associated tremor ataxia syndrome Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 2
Fragile X associated tremor ataxia syndrome Is a X-linked dominant hereditary disease 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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