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73119000: Retinitis pigmentosa-deafness-ataxia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
121439016 Retinitis pigmentosa-deafness-ataxia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
121440019 Hallgren's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
813472015 Retinitis pigmentosa-deafness-ataxia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
121439016 Retinitis pigmentosa-deafness-ataxia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
121439016 Retinitis pigmentosa-deafness-ataxia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
121440019 Hallgren's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
813472015 Retinitis pigmentosa-deafness-ataxia syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
813472015 Retinitis pigmentosa-deafness-ataxia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
647741000274117 Hallgren-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
647751000274119 Syndrom mit Retinitis pigmentosa, Taubheit und Ataxie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4629471000241118 syndrome de rétinite pigmentaire-surdité-ataxie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4629471000241118 syndrome de rétinite pigmentaire-surdité-ataxie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
647741000274117 Hallgren-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
647751000274119 Syndrom mit Retinitis pigmentosa, Taubheit und Ataxie 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
Retinitis pigmentosa-deafness-ataxia syndrome Is a Retinitis pigmentosa-deafness syndrome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Retinitis pigmentosa-deafness-ataxia syndrome Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept)
Retinitis pigmentosa-deafness-ataxia syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinitis pigmentosa-deafness-ataxia syndrome Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinitis pigmentosa-deafness-ataxia syndrome Finding site Structure of auditory system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Retinitis pigmentosa-deafness-ataxia syndrome Interprets Hearing true Inferred relationship Existential restriction modifier (core metadata concept) 3
Retinitis pigmentosa-deafness-ataxia syndrome Interprets entité observable fonctionnelle false Inferred relationship Existential restriction modifier (core metadata concept)
Retinitis pigmentosa-deafness-ataxia syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Retinitis pigmentosa-deafness-ataxia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Retinitis pigmentosa-deafness-ataxia syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Retinitis pigmentosa-deafness-ataxia syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Retinitis pigmentosa-deafness-ataxia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Retinitis pigmentosa-deafness-ataxia syndrome Finding site Structure of auditory system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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