Amino acid change:Find:Pt:Bld/Tiss:Nom:Molgen

Preferred Label : Amino acid change:Find:Pt:Bld/Tiss:Nom:Molgen;

LOINC status : ACTIVE;

LOINC display name : Amino acid change Molgen Nom (Bld/Tiss);

LOINC long common name : Amino acid change (pHGVS);

LOINC short name : Amino acid change;

LOINC description : Human Genome Variation Society (HGVS) nomenclature for an amino acid sequence. This value is derivable from the DNA Marker value if available. It is provided for convenience. The use of the nomenclature must be extended to describe non-variations (aka. wild types) see samples for wild type examples.;

Détails

Origin ID

48005-3;

UMLS CUI

C1953352;

Has component
- Amino acid change [LOINC component]
Has method
- Molecular genetics [LOINC method]
Has property
- Finding [LOINC Property]
Has scale
- Nom [LOINC scale]
Has system
- Blood [LOINC System]
- Blood or Tissue [LOINC System]
- Tissue and Smears [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Part of panel
- DNA analysis discrete sequence variation panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
- DNA marker assessed panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
- DNA marker identified panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
- Sequence variation panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
- Simple variant panel:-:Pt:^Patient:-: [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Position du mot-clé dans l'(les) arborescence(s) :

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