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715726000: Spinocerebellar ataxia type 7 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3303530011 Spinocerebellar ataxia type 7 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3303531010 Spinocerebellar ataxia type 7 en Synonym Active Entire term case insensitive SNOMED CT core module
3303532015 Ataxia with pigmentary retinopathy en Synonym Active Entire term case insensitive SNOMED CT core module
3303533013 Cerebellar syndrome pigmentary maculopathy 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 7 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 7 Is a Hereditary cerebellar degeneration false Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 7 Is a Spinocerebellar ataxia true Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 7 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 7 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 3
Spinocerebellar ataxia type 7 Finding site Spinal cord structure false Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 7 Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 3
Spinocerebellar ataxia type 7 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 7 Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 7 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 7 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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