@prefix dcterms: .
@prefix dcat: .
@prefix foaf: .
@prefix xsd: .
@prefix ldp: .
a dcat:Resource,
dcat:Dataset;
dcat:keyword "Rare hepatic disease"@en, "Rare immune disease"@en, "Rare inborn errors of metabolism"@en,
"Rare infectious disease"@en, "Rare infertility"@en, "Rare maxillo-facial surgical disease"@en,
"Rare neoplastic disease"@en, "Rare neurologic disease"@en, "Rare odontologic disease"@en,
"Rare ophthalmic disorder"@en, "Rare otorhinolaryngologic disease"@en, "Rare renal disease"@en,
"Rare respiratory disease"@en, "Rare skin disease"@en, "Rare surgical cardiac disease"@en,
"Rare surgical thoracic disease"@en, "Rare systemic or rheumatologic disease"@en,
"Rare teratologic disease"@en, "Rare urogenital disease"@en, "Rare diseases"@en, "Maladies rares"@fr,
"Zeldzame ziekten"@nl, "Epidemiology"@en, "Orphanet"@en, "Population-based registry"@en,
"Rare abdominal surgical disease"@en, "Rare allergic disease"@en, "Rare bone disease"@en,
"Rare cardiac disease"@en, "Rare circulatory system disease"@en, "Rare developmental defect during embryogenesis"@en,
"Rare disorder due to toxic effects"@en, "Rare disorder potentially indicated for transplant or complication after transplantation"@en,
"Rare disorder without a determined diagnosis after full investigation"@en, "Rare endocrine disease"@en,
"Rare gastroenterologic disease"@en, "Rare genetic disease"@en, "Rare gynecologic or obstetric disease"@en,
"Rare hematologic disease"@en;
dcat:landingPage ;
dcat:theme ;
;
"120"^^xsd:nonNegativeInteger;
"0"^^xsd:nonNegativeInteger;
"The target population of the CRRD comprises individuals affected by a rare disease whose care pathway involves consultation with an accredited genetic centre or Rare Disease Function in Belgium."@en;
;
dcterms:alternative "CRRD"@en;
dcat:distribution ;
;
, ,
, , ,
;
,
, ,
, ,
;
"Central Registry of Rare Diseases";
foaf:page , ;
dcterms:description "Le Registre Central des Maladies Rares (CRRD) est une base de données nationale contenant un ensemble de données minimal, pseudonymisé et transversal concernant des patients ayant consulté un centre d’expertise en Belgique pour une maladie rare. Le registre comprend des patients présentant un diagnostic confirmé de maladie rare, ainsi que des patients pour lesquels tous les efforts diagnostiques raisonnables, menés par des experts des maladies rares à l’aide de méthodes de pointe et des capacités diagnostiques disponibles, n’ont pas abouti à un diagnostic concluant d’une affection cliniquement reconnue. En Europe, une maladie est considérée comme rare lorsque sa prévalence est inférieure à 5 cas pour 10,000 habitants, et à ce jour plus de 6,500 maladies rares différentes ont été identifiées. Les données du CRRD sont fournies par les huit centres de génétique humaine agréés et les huit Fonctions Maladies Rares. Le registre soutient la surveillance nationale de la santé publique, l’élaboration des politiques et la recherche scientifique dans le domaine des maladies rares."@fr,
"Het Centraal Register Zeldzame Ziekten (CRRD) is een nationale databank die een minimale, gepseudonimiseerde en transversale dataset bevat over patiënten die in België een expertisecentrum voor een zeldzame ziekte hebben geraadpleegd. Het register omvat zowel patiënten met een bevestigde diagnose van een zeldzame ziekte als patiënten bij wie, ondanks alle redelijke diagnostische inspanningen door experten in zeldzame ziekten met het gebruik van de meest geavanceerde methoden en beschikbare diagnostische mogelijkheden, geen sluitende diagnose van een klinisch erkende aandoening kon worden gesteld. In Europa wordt een ziekte als zeldzaam beschouwd wanneer de prevalentie lager is dan 5 gevallen per 10,000 inwoners, en tot op heden zijn meer dan 6,500 verschillende zeldzame ziekten geïdentificeerd. Gegevens in het CRRD worden aangeleverd door de acht erkende genetische centra en de acht Functies Zeldzame Ziekten. Het register ondersteunt nationale monitoring van de volksgezondheid, beleidsontwikkeling en wetenschappelijk onderzoek op het gebied van zeldzame ziekten."@nl,
"The Central Registry of Rare Diseases (CRRD) is a national database containing a minimal, pseudonymised, cross-sectional dataset on patients who have consulted an expert centre in Belgium for a rare disease. The registry includes patients with a confirmed rare disease diagnosis, as well as patients for whom all reasonable diagnostic efforts by rare disease experts, using state-of-the-art methods and available diagnostic capabilities, did not result in a conclusive diagnosis of a clinically recognised condition. In Europe, a disease is considered rare when its prevalence is below 5 cases per 10,000 inhabitants, and to date more than 6,500 different rare diseases have been identified. Data in the CRRD are provided by the eight accredited genetic centres and the eight Rare Diseases Functions. The registry supports national public health monitoring, policy development, and scientific research in the field of rare diseases."@en;
dcterms:publisher [ a foaf:Agent;
dcterms:type ;
[ a ;
;
];
foaf:name "Sciensano";
dcterms:description "Sciensano is a public and independent scientific institute dedicated to human and animal health and their environment. Sciensano conducts scientific research and surveillance, and supports the government and various agencies and organisations with health expertise, advice and services."@en
];
dcterms:title "Central Registry of Rare Diseases"@en, "Registre Central des Maladies Rares"@fr,
"Centraal Register Zeldzame Ziekten"@nl;
dcterms:accessRights ;
dcterms:conformsTo , ;
dcterms:identifier "https://sciensanofdp.darwinproject.be/metadata.py?meta=https://intranet-fdp.sciensano.be/dataset/970828b6-ced7-4a58-ac44-845286687d99"^^xsd:anyURI;
dcterms:language ,
, ;
dcterms:license ;
;
"2026-07-23T23:01:55.757Z"^^xsd:dateTime;
"2026-07-23T23:02:02.554Z"^^xsd:dateTime;
,
;
dcterms:isPartOf ;
"2026-07-23T23:01:51.000Z"^^xsd:dateTime;
;
;
;
;
dcterms:provenance ;
dcterms:spatial ;
dcterms:type ;
,
, ,
, ;
dcat:contactPoint .
;
.
;
.
a ;
dcterms:identifier "https://public-fdp.sciensano.be/dataset/4b1e7ee6-6b00-40b3-8c9c-8fa2a1f25122" .
a dcterms:Location .
a dcterms:RightsStatement .
a ;
"""
Health"""@en .
a ;
"""
Personal Data"""@en .
a dcterms:LinguisticSystem .
a .
a ;
"""
Population-based health data registries (public health registries)"""@en .
a dcterms:LinguisticSystem .
a dcterms:LinguisticSystem .
a .
a .
a .
a ;
"EMA";
"https://catalogues.ema.europa.eu/node/4030/quantitative-descriptors"^^xsd:anyURI .
a ;
"Belgian Health Data Agency";
"https://catalog.hda.belgium.be/dataset/urn:li:dataset:(urn:li:dataPlatform:Sciensano,Central%20registry%20for%20rare%20diseases,PROD)/Schema?is_lineage_mode=false&schemaFilter="^^xsd:anyURI .
a ;
"FAIR Data Point for metadata on Sciensano's scientific and health data";
"https://sciensano.healthdataportal.eu:443/dataset/13710174-c535-4525-9527-f266635497e8"^^xsd:anyURI .
a ;
"FAIR.healthdata.be";
"https://fair.healthdata.be/dataset/a36012ab-8ab5-4fcf-b86c-c5c191ad14b0"^^xsd:anyURI .
a ,
;
"Health services research - Rare diseases team (Sciensano)";
;
"Sciensano";
"Health services research" .
a ;
dcterms:source ;
dcterms:description "For research involving special categories of sensitive personal data, Article 9(2)(j) of the GDPR establishes a specific legal basis for scientific, historical, or statistical research."@en .
a dcterms:ProvenanceStatement;
"Data in the CRRD originate from the eight accredited genetic centres and the eight Rare Diseases Functions in Belgium."@en .
a ;
dcterms:description "To support national public health monitoring, policy development, and scientific research in the field of rare diseases."@en .
a dcterms:Standard .
a dcterms:Standard .
a dcterms:Standard .
a dcterms:Standard .
a dcterms:Standard .
a dcterms:Standard .
a dcterms:Standard .
a ;
"https://intranet-fdp.sciensano.be/dataset/970828b6-ced7-4a58-ac44-845286687d99"^^xsd:anyURI .
a .
a .
a .
a foaf:Document .
a ldp:DirectContainer;
dcterms:title "Distributions";
ldp:membershipResource ;
ldp:hasMemberRelation dcat:distribution;
ldp:contains .
a ldp:DirectContainer;
dcterms:title "Samples";
ldp:membershipResource ;
ldp:hasMemberRelation ;
ldp:contains .
a ldp:DirectContainer;
dcterms:title "Analytics";
ldp:membershipResource ;
ldp:hasMemberRelation .
"Dataset Profile" .