mutation - CISMeF

Preferred Label : mutation;

IUPAC definition : A heritable change in the nucleotide sequence of genomic DNA (or RNA in RNA viruses), or in the number of genes or chromosomes in a cell, which may occur spontaneously or be brought about by chemical mutagens or by radiation (induced mutation).;

Details

Origin ID

M04074;

Automatic exact mappings (from CISMeF team)
- Gene Variant Negative [NCIt concept]
- Gene Variant Positive [NCIt concept]
- Mutate [NCIt concept]
- Mutation ID [EDAM data]
- Mutations [LOINC component]
- Mutism (finding) [SNOMED CT concept]
- Serine-Protein Kinase ATM [NCIt concept]
- mutation [COVID-19 Thesaurus concept]
- mutation [Blood Transfusion thesaurus concept]
- point mutation [MeSH Descriptor]
Currated CISMeF NLP mapping
- Mutation Abnormality [NCIt concept]
- Mutations [LOINC Class]
- mutation [MeSH Descriptor]
- mutation [MeSH concept]
See also
- RNA [IUPAC Term]
- chromosome [IUPAC Term]
- deoxyribonucleic acids [IUPAC Term]
- frame-shift mutation [IUPAC Term]
- gene (cistron) [IUPAC Term]
- genetic algorithm [IUPAC Term]
- genetic code [IUPAC Term]
- mutagen [IUPAC Term]
- mutagenesis [IUPAC Term]
- mutation rate [IUPAC Term]
- nucleotides [IUPAC Term]
- ribonucleic acids [IUPAC Term]
- sequence [IUPAC Term]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
- Genetic Function [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients