MII IG Kerndatensatz-Modul Seltene Erkrankungen
2027.0.0-ballot -
Germany
This page is part of the MII Implementation Guide Seltene Erkrankungen (v2027.0.0-ballot: 2027 Ballot 1) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions
German
status: Final
category: Laboratory
code: Genetic variant assessment
effective: 2024-08-25
value: Positive
note:
Heterozygoter Anlagetraeger fuer F508del. Eine zweite CFTR-Mutation wurde bei vollstaendiger Genanalyse nicht gefunden. Mukoviszidose damit ausgeschlossen; die IRT-Erhoehung im Screening war transient.
component
code: Gene studied [ID]
value: CFTR
component
code: Genomic source class
value: Germline
component
code: DNA change (c.HGVS)
value: c.1521_1523del
component
code: Amino acid change (pHGVS)
value: p.Phe508del
component
code: Allelic state
value: Heterozygous