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719250005: Spinocerebellar ataxia type 18 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3315683016 Spinocerebellar ataxia type 18 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3315684010 Spinocerebellar ataxia type 18 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
Spinocerebellar ataxia type 18 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 18 Is a Hereditary cerebellar degeneration false Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 18 Is a Spinocerebellar ataxia true Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 18 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 18 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 3
Spinocerebellar ataxia type 18 Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 18 Finding site Spinal cord structure false Inferred relationship Existential restriction modifier 3
Spinocerebellar ataxia type 18 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 18 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 18 Finding site Spinal cord 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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