MII VS SE Genetic Basis (retired) - MII IG Kerndatensatz-Modul Seltene Erkrankungen v2027.0.0-ballot

MII IG Kerndatensatz-Modul Seltene Erkrankungen
2027.0.0-ballot - Germany

MII IG Kerndatensatz-Modul Seltene Erkrankungen - Downloaded Version 2027.0.0-ballot See the Directory of published versions

ValueSet: MII VS SE Genetic Basis (retired)

Official URL: https://www.medizininformatik-initiative.de/fhir/ext/modul-seltene/ValueSet/mii-vs-seltene-genetic-basis				Version: 2027.0.0-ballot
Retired as of 2026-09-14				Computable Name: MII_VS_Seltene_GeneticBasis

RETIRED. Nicht verwenden. Acht der neun enthaltenen SNOMED-Codes bezeichnen etwas anderes als ihr Display behauptet oder existieren nicht; das ValueSet muss neu erstellt werden.

References

This value set is not used here; it may be used elsewhere (e.g. specifications and/or implementations that use this content)

Logical Definition (CLD)

Profiles: CRMI Shareable ValueSet, CRMI Publishable ValueSet

Include these codes as defined in http://snomed.info/sct version Not Stated (use latest from terminology server)

Code	Display
409709004	Chromosomal disorder
264530000	Single gene disorder
16402000	Mitochondrial disorder
268298002	Polygenic disorder
429962007	Disorder due to copy number variation
718211000119104	Disorder due to trinucleotide repeat expansion
416010008	Disorder due to uniparental disomy
429252008	Disorder due to genomic imprinting
363235000	Multifactorial disorder

Expansion

Expansions are not generated for retired value sets

Description of the above table(s).

IG © 2022+ Medizininformatik Initiative. Package de.medizininformatikinitiative.kerndatensatz.seltene#2027.0.0-ballot based on FHIR 4.0.1. Generated 2026-09-14
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