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57838006: Retinitis pigmentosa-deafness 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
96172019 Retinitis pigmentosa-deafness syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
96173012 Usher's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
796504017 Retinitis pigmentosa-deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1231772018 Usher syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1676521000052115 Ushers syndrom sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinitis pigmentosa-deafness syndrome Is a Multisystem disorder U-V false Inferred relationship Some
Retinitis pigmentosa-deafness syndrome Is a Retinitis pigmentosa false Inferred relationship Some
Retinitis pigmentosa-deafness syndrome Finding site Retinal structure false Inferred relationship Some
Retinitis pigmentosa-deafness syndrome Is a multisystemsjukdom false Inferred relationship Some
Retinitis pigmentosa-deafness syndrome Associated morphology Dystrophy true Inferred relationship Some 1
Retinitis pigmentosa-deafness syndrome Finding site Retinal structure true Inferred relationship Some 1
Retinitis pigmentosa-deafness syndrome Is a Autosomal recessive retinitis pigmentosa true Inferred relationship Some
Retinitis pigmentosa-deafness syndrome Is a Congenital malformation true Inferred relationship Some
Retinitis pigmentosa-deafness syndrome Is a Auditory system hereditary disorder true Inferred relationship Some
Retinitis pigmentosa-deafness syndrome Is a Congenital sensorineural hearing loss (disorder) true Inferred relationship Some
Retinitis pigmentosa-deafness syndrome Finding site Structure of auditory system (body structure) false Inferred relationship Some
Retinitis pigmentosa-deafness syndrome Interprets Hearing true Inferred relationship Some 3
Retinitis pigmentosa-deafness syndrome Interprets observabel som rör funktion false Inferred relationship Some
Retinitis pigmentosa-deafness syndrome Associated morphology utvecklingsabnormitet false Inferred relationship Some 2
Retinitis pigmentosa-deafness syndrome Occurrence Congenital true Inferred relationship Some 2
Retinitis pigmentosa-deafness syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Retinitis pigmentosa-deafness syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Retinitis pigmentosa-deafness syndrome Occurrence Congenital true Inferred relationship Some 4
Retinitis pigmentosa-deafness syndrome Finding site Structure of auditory system (body structure) true Inferred relationship Some 4
Retinitis pigmentosa-deafness syndrome Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Usher syndrome type 1 Is a True Retinitis pigmentosa-deafness syndrome Inferred relationship Some
Usher syndrome type 2 (disorder) Is a True Retinitis pigmentosa-deafness syndrome Inferred relationship Some
Retinitis pigmentosa-deafness-ataxia syndrome Is a True Retinitis pigmentosa-deafness syndrome Inferred relationship Some
Retinitis pigmentosa-deafness syndrome type 3 (disorder) Is a True Retinitis pigmentosa-deafness syndrome Inferred relationship Some

This concept is not in any reference sets

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