FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

719207000: Spinocerebellar ataxia type 11 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
5402005010 A rare neurologic disease that is characterized by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402006011 A rare neurologic disease that is characterised by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3315417015 Spinocerebellar ataxia type 11 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315418013 Spinocerebellar ataxia type 11 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
887271000172114 SCA11 - spinocerebellar ataxia type 11 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
951981000172110 ataxie spinocérébelleuse type 11 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3396061001000116 Ataxie, spinozerebelläre, Typ 11 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare neurologic disease that is characterized by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs. Is a Autosomal dominant hereditary disorder (disorder) true Inferred relationship Some
A rare neurologic disease that is characterized by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs. Is a Hereditary cerebellar degeneration false Inferred relationship Some
A rare neurologic disease that is characterized by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs. Is a Spinocerebellar ataxia true Inferred relationship Some
A rare neurologic disease that is characterized by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs. Associated morphology dégénérescence false Inferred relationship Some 2
A rare neurologic disease that is characterized by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs. Associated morphology dégénérescence false Inferred relationship Some 3
A rare neurologic disease that is characterized by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs. Finding site Cerebellar structure true Inferred relationship Some 2
A rare neurologic disease that is characterized by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs. Finding site Spinal cord structure false Inferred relationship Some 3
A rare neurologic disease that is characterized by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs. Associated morphology Degenerative abnormality true Inferred relationship Some 2
A rare neurologic disease that is characterized by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs. Associated morphology Degenerative abnormality true Inferred relationship Some 1
A rare neurologic disease that is characterized by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs. Finding site Spinal cord structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start