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719255000: Spinocerebellar ataxia type 34 (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
3315698019 Spinocerebellar ataxia type 34 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3315699010 Spinocerebellar ataxia type 34 en Synonym Active Entire term case insensitive SNOMED CT core module
3315700011 Erythrokeratodermia with ataxia en Synonym Active Entire term case insensitive SNOMED CT core module
3315701010 Spinocerebellar ataxia and erythrokeratodermia 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 34 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 34 Is a Hereditary cerebellar degeneration false Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 34 Is a Spinocerebellar ataxia true Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 34 Is a Erythrokeratoderma true Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 34 Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 34 Has definitional manifestation Abnormal keratinization false Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 34 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 6
Spinocerebellar ataxia type 34 Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 6
Spinocerebellar ataxia type 34 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 4
Spinocerebellar ataxia type 34 Finding site Spinal cord structure false Inferred relationship Existential restriction modifier 4
Spinocerebellar ataxia type 34 Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 5
Spinocerebellar ataxia type 34 Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Spinocerebellar ataxia type 34 Finding site Skin structure false Inferred relationship Existential restriction modifier 5
Spinocerebellar ataxia type 34 Is a Congenital anomaly of skin true Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 34 Interprets Keratinization, function true Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 34 Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 34 Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 34 Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 34 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 34 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 34 Is a Functional finding false Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 34 Is a Keratosis false Inferred relationship Existential restriction modifier
Spinocerebellar ataxia type 34 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 4
Spinocerebellar ataxia type 34 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 3
Spinocerebellar ataxia type 34 Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 3
Spinocerebellar ataxia type 34 Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 4
Spinocerebellar ataxia type 34 Is a Developmental hereditary disorder 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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