MSH2 gene MLH1 gene MSH6 gene mutation analysis limited to known familial mutations:Find:Pt:Bld/Tiss:Doc:Molgen

Preferred Label : MSH2 gene MLH1 gene MSH6 gene mutation analysis limited to known familial mutations:Find:Pt:Bld/Tiss:Doc:Molgen;

LOINC status : ACTIVE;

LOINC display name : MSH2 gene MLH1 gene MSH6 gene familial mut analysis Molgen Doc (Bld/Tiss);

LOINC long common name : MSH2 gene MLH1 gene MSH6 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method;

LOINC short name : MSH2 MLH1 MSH6 gene Fam Mut Anl Bld/T;

LOINC description : This term is used for carrier or diagnostic testing for at-risk or presymptomatic relatives of an affected individual who has a previously identified known genetic mutation within the MLH1, MSH2 or MSH6 genes. Mutations in these genes cause hereditary nonpolyposis colorectal cancer (HNPCC). Mutation analysis only includes testing for the known familial mutation.;

Details

Origin ID

76063-7;

UMLS CUI

C3869971;

Has component
- Gene [LOINC component]
- Gene mutation analysis limited to known familial mutations [LOINC component]
- MLH1 gene [LOINC component]
- MSH2 gene [LOINC component]
- MSH2 gene+MLH1 gene [LOINC component]
- MSH2 gene+MLH1 gene+MSH6 gene [LOINC component]
- MSH2 gene+MLH1 gene+MSH6 gene mutation analysis limited to known familial mutations [LOINC component]
- MSH6 gene [LOINC component]
- Mutations [LOINC component]
Has method
- Molecular genetics [LOINC method]
Has property
- Finding [LOINC Property]
Has scale
- Doc [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]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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