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1208512000: Spinocerebellar ataxia type 41 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Mar 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4964978016 Spinocerebellar ataxia type 41 en Synonym Active Entire term case insensitive SNOMED CT core module
4964979012 Spinocerebellar ataxia type 41 (disorder) en Fully specified name 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 41 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 41 Is a Spinocerebellar ataxia true Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 41 Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 41 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 41 Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 41 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 41 Is a Chronic brain syndrome true Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 41 Clinical course Progressive true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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