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1010610007: Retinitis pigmentosa-deafness syndrome type 3 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4213324014 Usher syndrome type 3 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4279326016 Retinitis pigmentosa-deafness syndrome type 3 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4279327013 Retinitis pigmentosa-deafness syndrome type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
7698161000241110 syndrome USH3 (Usher 3) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7698171000241119 syndrome d'Usher de type 3 fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7698181000241117 syndrome de rétinite pigmentaire et surdité, de type 3 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
512651000274111 Syndrom mit Retinitis pigmentosa und Taubheit, Typ 3 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
554271000274116 Usher-Syndrom, Typ 3 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 syndrome type 3 (disorder) Is a Retinitis pigmentosa-deafness syndrome true Inferred relationship Some
Retinitis pigmentosa-deafness syndrome type 3 (disorder) Finding site Structure of auditory system (body structure) true Inferred relationship Some 1
Retinitis pigmentosa-deafness syndrome type 3 (disorder) Occurrence Congenital true Inferred relationship Some 1
Retinitis pigmentosa-deafness syndrome type 3 (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Retinitis pigmentosa-deafness syndrome type 3 (disorder) Occurrence Congenital true Inferred relationship Some 2
Retinitis pigmentosa-deafness syndrome type 3 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Retinitis pigmentosa-deafness syndrome type 3 (disorder) Interprets Hearing true Inferred relationship Some 3
Retinitis pigmentosa-deafness syndrome type 3 (disorder) Finding site Retinal structure true Inferred relationship Some 4
Retinitis pigmentosa-deafness syndrome type 3 (disorder) Associated morphology Dystrophy true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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