ARCHETYPE Phenopacket IscnAllele (openEHR-EHR-CLUSTER.pp_iscnallele.v0)

ARCHETYPE IDopenEHR-EHR-CLUSTER.pp_iscnallele.v0
ConceptPhenopacket IscnAllele
DescriptionIscnAllele
PurposeThis element can be used to describe cytogenetic anomalies according to the International System for Human Cytogenetic Nomenclature (ISCN), an international standard for human chromosome nomenclature, which includes band names, symbols and abbreviated terms used in the description of human chromosome and chromosome abnormalities. For example del(6)(q23q24) describes a deletion from band q23 to q24 on chromosome 6.
References
Copyright© openEHR Foundation
AuthorsAuthor name: Heather Leslie
Organisation: Atomica Informatics
Email: heather.leslie@atomicainformatics.com
Date originally authored: 2019-09-25
Other Details LanguageAuthor name: Heather Leslie
Organisation: Atomica Informatics
Email: heather.leslie@atomicainformatics.com
Date originally authored: 2019-09-25
OtherDetails Language Independent{licence=This work is licensed under the Creative Commons Attribution-ShareAlike 3.0 License. To view a copy of this license, visit http://creativecommons.org/licenses/by-sa/3.0/., custodian_organisation=openEHR Foundation, original_namespace=org.openehr, original_publisher=openEHR Foundation, custodian_namespace=org.openehr, MD5-CAM-1.0.1=18A39E90706B58785C26F922EA673337, build_uid=2d88227b-6077-4c44-98b5-8a9cfe116f76, revision=0.0.1-alpha}
Keywords
Lifecyclein_development
UIDde663a9c-d89d-47b5-abab-a0748a3fc9d8
Language useden
Citeable Identifier1013.1.4154
Revision Number0.0.1-alpha
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