FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

771514002: Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3706577019 Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706578012 Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706579016 A genetic neurodegenerative disease with normal early development followed by childhood onset optic atrophy with progressive vision loss and eventually blindness, followed by progressive neurological decline that typically includes cerebellar ataxia, nystagmus, dorsal column dysfunction (decreased vibration and position sense), spastic paraplegia and finally tetraparesis. There is evidence this disease is caused by homozygous or compound heterozygous mutation in the UCHL1 gene on chromosome 4p13. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3706577019 Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706578012 Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3706579016 A genetic neurodegenerative disease with normal early development followed by childhood onset optic atrophy with progressive vision loss and eventually blindness, followed by progressive neurological decline that typically includes cerebellar ataxia, nystagmus, dorsal column dysfunction (decreased vibration and position sense), spastic paraplegia and finally tetraparesis. There is evidence this disease is caused by homozygous or compound heterozygous mutation in the UCHL1 gene on chromosome 4p13. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
544781000274111 Autosomal-rezessive spastische Paraplegie, Typ 79 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3427751001000119 Früh beginnende progressive Neurodegeneration-Blindheit-Ataxie-Spastik-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1005901000172119 syndrome de neurodégénérescence progressive de l'enfant-cécité-ataxie-spasticité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1005901000172119 syndrome de neurodégénérescence progressive de l'enfant-cécité-ataxie-spasticité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
544781000274111 Autosomal-rezessive spastische Paraplegie, Typ 79 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3427751001000119 Früh beginnende progressive Neurodegeneration-Blindheit-Ataxie-Spastik-Syndrom 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
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) Associated morphology Primary atrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) Is a Hereditary optic atrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) Is a Inherited optic neuropathy (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) Is a Chronic nervous system disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) Is a Degenerative disease of the central nervous system false Inferred relationship Existential restriction modifier (core metadata concept)
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) Finding site Optic nerve structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) Occurrence Childhood false Inferred relationship Existential restriction modifier (core metadata concept) 2
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept) 2
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) Occurrence Childhood true Inferred relationship Existential restriction modifier (core metadata concept) 1
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) Is a Hereditary ataxia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 2
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start