Rekvisitionsblanket for patientgruppen Arvelige hjertesygdomme. 

Rekvisitionsblanket - Arvelige hjertesygdomme

Information til rekvirenter

Rekvisitionsblanket for patientgruppen Arvelig hæmatologisk sygdom. 

Rekvisitionsblanket - Arvelig hæmatologisk sygdom

Information til rekvirenter

Rekvisitionsblanket for patientgruppen Audiogenetik. 

Rekvisitionsblanket - Audiogenetik

Information til rekvirenter

Rekvisitionsblanket for patientgruppen Endokrinologiske patienter. 

Rekvisitionsblanket - Endokrinologiske patienter

Information til rekvirenter

Rekvisitionsblanket for patientgruppen Børn og unge med kræft. 

Rekvisitionsblanket - Børn og unge med kræft (germline)

Rekvisitionsblanket - Børn og unge med kræft (somatisk)

Information til rekvirenter

Rekvisitionsblanket for patientgruppen Kræft hos unge voksne (18-30 år) samt arvelig kræft hos voksne.

Rekvisitionsblanket - Kræft hos unge voksne (18-30 år) samt arvelig kræft hos voksne (germline)

Rekvisitionsblanket - Kræft hos unge voksne (18-30 år) samt arvelig kræft hos voksne (somatisk)

Information til rekvirenter

Rekvisitionsblanket for patientgruppen Neurogenetiske patienter.

Rekvisitionsblanket - Neurogenetiske patienter

Information til rekvirenter

Rekvisitionsblanket for patientgruppen Nyresvigt. 

Rekvisitionsblanket - Nyresvigt

Information til rekvirenter

Rekvisitionsblanket for patientgruppen Oftalmologi.

Rekvisitionsblanket - Oftalmologi

Information til rekvirenter

Rekvisitionsblanket for patientgruppen Primær immundefekt. 

Rekvisitionsblanket - Primær immundefekt

Information til rekvirenter

Rekvisitionsblanket for patientgruppen for Sjældne sygdomme hos børn og unge under 18 år

Rekvisitionsblanket - Sjældne sygdomme hos børn og unge under 18 år

Information til rekvirenter

Rekvisitionsblanket for patientgruppen Sjældne sygdomme hos voksne.

Rekvisitionsblanket - Sjældne sygdomme hos voksne

Information til rekvirenter

Rekvisitionsblanket for patientgruppen Uhelbredelig kræft

Rekvisitionsblanket - Udbredt og uhelbredelig kræft (germline)

Rekvisitionsblanket - Udbredt og uhelbredelig kræft (somatisk)

Information til rekvirenter

Dansk

Samtykkeblanketten skal ikke sendes til Nationalt Genom Center men til den rekvirerende læge, der har underskrevet erklæringen.

Samtykkeblanket til patienter

Er du blevet tilbudt genetisk undersøgelse i forbindelse med fosterdiagnostik, skal du bruge nedenstående samtykkeblanket.

Samtykkeblanket i forbindelse med fosterdiagnostik

Engelsk

The consent form must not be sent to the Danish National Genome Center, but to the requesting doctor who signed the declaration.

Consent form for patients

If you have been offered a genetic test in connection with prenatal testing, you must use the consent form below.

Consent form in connection with prenatal testing

Arabisk

The consent form must not be sent to the Danish National Genome Center, but to the requesting doctor who signed the declaration.

Consent form for patients

If you have been offered a genetic test in connection with prenatal testing, you must use the consent form below.

Consent form in connection with prenatal testing

Polsk

The consent form must not be sent to the Danish National Genome Center, but to the requesting doctor who signed the declaration.

Consent form for patients

If you have been offered a genetic test in connection with prenatal testing, you must use the consent form below.

Consent form in connection with prenatal testing

Tyrkisk

The consent form must not be sent to the Danish National Genome Center, but to the requesting doctor who signed the declaration.

Consent form for patients

If you have been offered a genetic test in connection with prenatal testing, you must use the consent form below.

Consent form in connection with prenatal testing

Urdu

The consent form must not be sent to the Danish National Genome Center, but to the requesting doctor who signed the declaration.

Consent form for patients

If you have been offered a genetic test in connection with prenatal testing, you must use the consent form below.

Consent form in connection with prenatal testing

Somalisk

The consent form must not be sent to the Danish National Genome Center, but to the requesting doctor who signed the declaration.

Consent form for patients

If you have been offered a genetic test in connection with prenatal testing, you must use the consent form below.

Consent form in connection with prenatal testing

Dansk

Information om, hvad gener er, og hvad der skal ske, og nogle af de valg, der skal træffes i sammenhæng med afgivelse af informeret samtykke til behandling, som indebærer en genetisk analyse (samtykkeblanket). Denne skriftlige information ledsages af en samtale.

Patientinformation vedrørende omfattende genetisk analyse

Foretages omfattende genetisk analyse i forbindelse med fosterdiagnostik, skal nedenstrående patientinformationsfolder bruges.

Information vedrørende omfattende genetisk analyse i forbindelse med fosterdiagnostik

Engelsk

Information regarding comprehensive genetic analysis

Patient information regarding comprehensive genetic analysis

If the genetic test is being conducted in the context of prenatal testing, you must use the information below.

Information concerning comprehensive genetic analysis in connection with prenatal testing

Arabisk

Information regarding comprehensive genetic analysis

Patient information regarding comprehensive genetic analysis

If the genetic test is being conducted in the context of prenatal testing, you must use the information below.

Information concerning comprehensive genetic analysis in connection with prenatal testing

Polsk

Information regarding comprehensive genetic analysis

Patient information regarding comprehensive genetic analysis

If the genetic test is being conducted in the context of prenatal testing, you must use the information below.

Information concerning comprehensive genetic analysis in connection with prenatal testing

Tyrkisk

Information regarding comprehensive genetic analysis

Patient information regarding comprehensive genetic analysis

If the genetic test is being conducted in the context of prenatal testing, you must use the information below.

Information concerning comprehensive genetic analysis in connection with prenatal testing

Urdu

Information regarding comprehensive genetic analysis

Patient information regarding comprehensive genetic analysis

If the genetic test is being conducted in the context of prenatal testing, you must use the information below.

Information concerning comprehensive genetic analysis in connection with prenatal testing

Somalisk

Information regarding comprehensive genetic analysis

Patient information regarding comprehensive genetic analysis

If the genetic test is being conducted in the context of prenatal testing, you must use the information below.

Information concerning comprehensive genetic analysis in connection with prenatal testing

Har du fået foretaget en helgenomanalyse i forbindelse med patientbehandling før den 1. maj 2019, kan du anmode Nationalt Genom Center om, at dine genetiske oplysninger opbevares på en sikker database i Nationalt Genom Centers supercomputersystem.

Blanket: Overførsel af genetiske oplysninger

Dansk

Ønsker du ikke, at dine genetiske oplysninger kan bruges til forskning, skal du tilmelde dig Vævsanvendelsesregisteret via nedenstående blanket. Blanketten gælder også, hvis den genetiske undersøgelse er foretaget af et foster i sammenhæng med en fosterdiagnostisk undersøgelse, og du ikke ønsker, at dine og dit fosters genetiske oplysninger kan bruges til forskning.

Til- og frameldelsesblanket Vævsanvendelsesregisteret

Engelsk

If you do not want your data to be used for research purposes, you must use the form below regarding registration in T​he National Database of Non-Consent to the Use of Tissue Samples for Scientific Purposes. The form also applies if the genetic test concerned a fetus in connection with prenatal testing, and you do not want the genetic data of you and your fetus to be used in research.

Registration and deregistration to T​he National Database of Non-Consent to the Use of Tissue Samples for Scientific Purposes

Arabisk

If you do not want your data to be used for research purposes, you must use the form below regarding registration in T​he National Database of Non-Consent to the Use of Tissue Samples for Scientific Purposes. The form also applies if the genetic test concerned a fetus in connection with prenatal testing, and you do not want the genetic data of you and your fetus to be used in research.

Registration and deregistration to T​he National Database of Non-Consent to the Use of Tissue Samples for Scientific Purposes

Polsk

If you do not want your data to be used for research purposes, you must use the form below regarding registration in T​he National Database of Non-Consent to the Use of Tissue Samples for Scientific Purposes. The form also applies if the genetic test concerned a fetus in connection with prenatal testing, and you do not want the genetic data of you and your fetus to be used in research.

Registration and deregistration to T​he National Database of Non-Consent to the Use of Tissue Samples for Scientific Purposes

Tyrkisk

If you do not want your data to be used for research purposes, you must use the form below regarding registration in T​he National Database of Non-Consent to the Use of Tissue Samples for Scientific Purposes. The form also applies if the genetic test concerned a fetus in connection with prenatal testing, and you do not want the genetic data of you and your fetus to be used in research.

Registration and deregistration to T​he National Database of Non-Consent to the Use of Tissue Samples for Scientific Purposes

Urdu

If you do not want your data to be used for research purposes, you must use the form below regarding registration in T​he National Database of Non-Consent to the Use of Tissue Samples for Scientific Purposes. The form also applies if the genetic test concerned a fetus in connection with prenatal testing, and you do not want the genetic data of you and your fetus to be used in research.

Registration and deregistration to T​he National Database of Non-Consent to the Use of Tissue Samples for Scientific Purposes

Somalisk

If you do not want your data to be used for research purposes, you must use the form below regarding registration in T​he National Database of Non-Consent to the Use of Tissue Samples for Scientific Purposes. The form also applies if the genetic test concerned a fetus in connection with prenatal testing, and you do not want the genetic data of you and your fetus to be used in research.

Registration and deregistration to T​he National Database of Non-Consent to the Use of Tissue Samples for Scientific Purposes

Vejledningen henvender sig til personale, der informerer patienter i forbindelse med indhentelse af skriftligt samtykke til patientbehandling, der indebærer omfattende genetisk analyse.

Vejledning til sundhedsfagligt personale

Vejledningen henvender sig til personale, der informerer patienter i forbindelse med indhentelse af skriftligt samtykke til patientbehandling, der indebærer omfattende genetisk analyse i sammenhæng med forsterdiagnostik.

Vejledning til sundhedsfagligt personale ifm. fosterdiagnostik (integreret i Sundhedsstyrelsens retningslinjer for fosterdiagnostik)

Dette er en brugervejledning, der beskriver indberetningsproceduren til Nationalt Genom Center. Brugervejledningen vil blive opdateret løbende, når der sker væsentlige ændringer i indberetningsprogrammet.

Vejledning om indberetning af oplysninger

Blanket til regioner, som skal benyttes i forbindelse med anmodning om overførsel af genetiske oplysninger til Nationalt Genom Center her. 

Blanket: Overførsel af genetiske oplysninger

Oplysning om behandlingen af dine genetiske oplysninger indsamlet i forbindelse med forskning

Oplysningsfolder til forsøgsdeltagere

Har du fået foretaget en omfattende genetisk analyse i forbindelse med forskning før den 1. maj 2019, kan du anmode Nationalt Genom Center om, at dine genetiske oplysninger opbevares på en sikker database i Nationalt Genom Centers supercomputersystem.

Blanket: Overførsel af genetiske oplysninger

Politik for patient- og borgerinddragelse i Nationalt Genom Center

Dansk

Habilitetspolitik og procedurer vedr. habilitetserklæringer for eksterne rådgivere/konsulenter, herunder medlemmer af udvalg/arbejdsgrupper nedsat af NGC. 

Habilitetspolitik og procedurer

Engelsk

Policy of impartiality and procedures concerning impartiality declaration for external advisors/consultants, including members of committees/working groups set up by the Danish National Genome Center and employees in the Danish National Genome Center.

Policy of impartiality and procedures

Dansk

Habilitetserklæring for personer, der skal bistå Nationalt Genom Center med at rådgive, undervise eller behandle sager.

Habilitetserklæring

Udfyldte habilitetserklæringer for arbejdsgrupper, specialistnetværk og advisory boards

Udfyldte habilitetserklæringer

Engelsk

Declaration of impartiality to persons that has to assist the Danish National Genome Center by counselling, teaching or processing cases.

Declaration of impartiality

Politik for refundering af rejseudgifter - eksterne

Rejse- og Udlægsafregning for eksterne under 24t

Rejse- og Udlægsafregning for eksterne over 24t