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719818007: X-linked spinocerebellar ataxia type 4 (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
3318021018 X-linked spinocerebellar ataxia type 4 (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3318022013 X-linked spinocerebellar ataxia type 4 en Synonym Active Entire term case sensitive SNOMED CT core module
3318023015 X-linked ataxia dementia syndrome 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
X-linked spinocerebellar ataxia type 4 Is a Hereditary cerebellar degeneration false Inferred relationship Existential restriction modifier
X-linked spinocerebellar ataxia type 4 Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
X-linked spinocerebellar ataxia type 4 Is a Spinocerebellar ataxia true Inferred relationship Existential restriction modifier
X-linked spinocerebellar ataxia type 4 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 2
X-linked spinocerebellar ataxia type 4 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 3
X-linked spinocerebellar ataxia type 4 Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 2
X-linked spinocerebellar ataxia type 4 Finding site Spinal cord structure false Inferred relationship Existential restriction modifier 3
X-linked spinocerebellar ataxia type 4 Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 1
X-linked spinocerebellar ataxia type 4 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
X-linked spinocerebellar ataxia type 4 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 2
X-linked spinocerebellar ataxia type 4 Is a X-linked recessive 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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