FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

718174008: Infantile striatonigral degeneration (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3310403014 Infantile striatonigral degeneration (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3310404015 Infantile striatonigral degeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311374010 Infantile bilateral striatal necrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311375011 Comprises of several syndromes of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus with characteristics of developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis. Can be familial or sporadic. The familial form has an insidious onset and a slowly progressive downhill course, while the sporadic form is associated with abrupt neurologic dysfunction following an acute systemic febrile illness such as a mycoplasma, measles or streptococcus infection. Familial disease can be inherited as an autosomal recessive or mitochondrial disorder. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Infantile striatonigral degeneration (disorder) morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
Infantile striatonigral degeneration (disorder) interprète (attribut) Movement (observable entity) true Inferred relationship Some 3
Infantile striatonigral degeneration (disorder) a pour interprétation (attribut) lent true Inferred relationship Some 3
Infantile striatonigral degeneration (disorder) est un(e) (attribut) dégénerescence striatonigrale true Inferred relationship Some
Infantile striatonigral degeneration (disorder) morphologie associée (attribut) dégénérescence false Inferred relationship Some 1
Infantile striatonigral degeneration (disorder) survenue (attribut) Infancy (qualifier value) true Inferred relationship Some 1
Infantile striatonigral degeneration (disorder) localisation d'une constatation (attribut) Structure of nigrostriate fiber (body structure) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Sporadic infantile bilateral striatal necrosis est un(e) (attribut) True Infantile striatonigral degeneration (disorder) Inferred relationship Some
Familial infantile bilateral striatal necrosis est un(e) (attribut) True Infantile striatonigral degeneration (disorder) Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

Back to Start