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514793471000119104: Usher-syndroom type 1F (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5181944018 Usher syndrome type 1F (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5181945017 Usher syndrome type 1F en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
14422101000146110 Usher-syndroom type 1F (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14422111000146112 syndroom van Usher type 1F nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14422121000146119 Usher-syndroom type 1F nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14486601000146112 syndroom van retinitis pigmentosa en doofheid type 1F nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Usher syndrome type 1F (disorder) Is a Usher syndrome type 1 true Inferred relationship Some
Usher syndrome type 1F (disorder) Interprets Hearing true Inferred relationship Some 4
Usher syndrome type 1F (disorder) Occurrence Congenital true Inferred relationship Some 2
Usher syndrome type 1F (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Usher syndrome type 1F (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Usher syndrome type 1F (disorder) Occurrence Congenital true Inferred relationship Some 3
Usher syndrome type 1F (disorder) Finding site Structure of auditory system (body structure) true Inferred relationship Some 3
Usher syndrome type 1F (disorder) Finding site Retinal structure true Inferred relationship Some 1
Usher syndrome type 1F (disorder) Associated morphology Dystrophy true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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