FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

734020000: Spinocerebellar ataxia type 40 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3481917012 Spinocerebellar ataxia type 40 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3481918019 Spinocerebellar ataxia type 40 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3481919010 A very rare disease with characteristics of adult-onset unsteady gait and dysarthria, followed by wide-based gait, gait ataxia, ocular dysmetria, intention tremor, scanning speech, hyperreflexia and dysdiadochokinesis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
977491000172111 SCA40 - spinocerebellar ataxia type 40 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
995501000172117 ataxie spinocérébelleuse type 40 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
875051000172111 spinocerebellaire ataxie type 40 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
902561000172111 SCA40 - spinocerebellaire ataxie type 40 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spinocerebellar ataxia type 40 (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Spinocerebellar ataxia type 40 (disorder) Is a Hereditary cerebellar degeneration false Inferred relationship Some
Spinocerebellar ataxia type 40 (disorder) Is a Spinocerebellar ataxia true Inferred relationship Some
Spinocerebellar ataxia type 40 (disorder) Associated morphology Degeneration false Inferred relationship Some 2
Spinocerebellar ataxia type 40 (disorder) Finding site Cerebellar structure false Inferred relationship Some 2
Spinocerebellar ataxia type 40 (disorder) Associated morphology Degeneration false Inferred relationship Some 3
Spinocerebellar ataxia type 40 (disorder) Finding site Spinal cord structure false Inferred relationship Some 3
Spinocerebellar ataxia type 40 (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 1
Spinocerebellar ataxia type 40 (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 2
Spinocerebellar ataxia type 40 (disorder) Finding site Cerebellar structure true Inferred relationship Some 1
Spinocerebellar ataxia type 40 (disorder) Finding site Spinal cord structure true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start