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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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinitis pigmentosa-deafness syndrome type 3 (disorder) est un(e) (attribut) syndrome associant rétinite pigmentaire et surdité true Inferred relationship Some
Retinitis pigmentosa-deafness syndrome type 3 (disorder) localisation d'une constatation (attribut) structure du système auditif true Inferred relationship Some 1
Retinitis pigmentosa-deafness syndrome type 3 (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Retinitis pigmentosa-deafness syndrome type 3 (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 2
Retinitis pigmentosa-deafness syndrome type 3 (disorder) survenue (attribut) congénital 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) interprète (attribut) Hearing, function (observable entity) true Inferred relationship Some 3
Retinitis pigmentosa-deafness syndrome type 3 (disorder) localisation d'une constatation (attribut) structure de la rétine true Inferred relationship Some 4
Retinitis pigmentosa-deafness syndrome type 3 (disorder) morphologie associée (attribut) Dystrophy (morphologic abnormality) 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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