FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

73119000: syndroom van retinitis pigmentosa, doofheid en ataxie (aandoening)


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
6955971000146118 syndroom van retinitis pigmentosa, doofheid en ataxie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6955981000146116 syndroom van retinitis pigmentosa, doofheid en ataxie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
9184151000146113 syndroom van Hallgren 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
Retinitis pigmentosa-deafness-ataxia syndrome Is a Retinitis pigmentosa-deafness syndrome true Inferred relationship Some
Retinitis pigmentosa-deafness-ataxia syndrome Finding site Retinal structure false Inferred relationship Some
Retinitis pigmentosa-deafness-ataxia syndrome Associated morphology Dystrophy true Inferred relationship Some 1
Retinitis pigmentosa-deafness-ataxia syndrome Finding site Retinal structure true Inferred relationship Some 1
Retinitis pigmentosa-deafness-ataxia syndrome Finding site Structure of auditory system (body structure) false Inferred relationship Some
Retinitis pigmentosa-deafness-ataxia syndrome Interprets Hearing true Inferred relationship Some 3
Retinitis pigmentosa-deafness-ataxia syndrome Interprets observatie betreffende functioneren false Inferred relationship Some
Retinitis pigmentosa-deafness-ataxia syndrome Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 2
Retinitis pigmentosa-deafness-ataxia syndrome Occurrence Congenital true Inferred relationship Some 2
Retinitis pigmentosa-deafness-ataxia syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Retinitis pigmentosa-deafness-ataxia syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Retinitis pigmentosa-deafness-ataxia syndrome Occurrence Congenital true Inferred relationship Some 4
Retinitis pigmentosa-deafness-ataxia syndrome Finding site Structure of auditory system (body structure) true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start