5-methyltetrahydrofolate-homocysteine s-methyltransferase

Preferred Label : 5-methyltetrahydrofolate-homocysteine s-methyltransferase;

Symbol : MTR;

CISMeF acronym : MTR;

Type : Gene;

Alternative titles and symbols : Tetrahydropteroylglutamate methyltransferase; Methionine synthase; MS;

Ensembl ID : ENSG00000116984;

Prefixed ID : *156570;

Details

Origin ID

156570;

UMLS CUI

C1417453;

Automatic exact mappings (from CISMeF team)
- 5-Methyltetrahydrofolate homocysteine methyltransferase [LOINC component]
- 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase [MeSH concept]
- 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase [MeSH Descriptor]
- 5-methyltetrahydrofolate-homocysteine methyltransferase [ORDO Gene]
- 5-methyltetrahydrofolate-homocysteine methyltransferase (substance) [SNOMED CT concept]
- GDC Menopause Status Terminology [NCIt concept]
- Homocystinuria without methylmalonic aciduria [ICD-11 More detail]
- INRG Stage MS [NCIt concept]
- MTR wt Allele [NCIt concept]
- Mass Spectrometer [NCIt concept]
- Mass Spectrometry [NCIt concept]
- Master of Science [NCIt concept]
- Methionine Synthase [NCIt concept]
- Metric System [NCIt concept]
- Microbiology Susceptibility Domain [NCIt concept]
- Millisecond [NCIt concept]
- Millisecond (qualifier value) [SNOMED CT concept]
- Mississippi [NCIt concept]
- Mitral valve stenosis [ICD-11 Category]
- Multiple sclerosis [ICD-11 Category]
- Multiple sclerosis [MedDRA Preferred Term]
- marginal sulcus [UBERON concept]
- multiple sclerosis [MedlinePlus Topic]
Currated CISMeF NLP mapping
- 5-methyltetrahydrofolate-homocysteine methyltransferase [HGNC gene]
- MTR Gene [NCIt concept]
- MTR gene [LOINC component]
False automatic mappings
- Montserrat [NCIt concept]
HGNC gene
- 5-methyltetrahydrofolate-homocysteine methyltransferase [HGNC gene]
NCIt concept(s)
- MTR Gene [NCIt concept]
- MTR wt Allele [NCIt concept]
- Methionine Synthase [NCIt concept]
ORDO concept(s)
- 5-methyltetrahydrofolate-homocysteine methyltransferase [ORDO Gene]
Phenotypes related
- Homocystinuria-megaloblastic anemia, cblg complementation type [OMIM Phenotype]
- Neural tube defects, folate-sensitive [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- 5-methyltetrahydrofolate-homocysteine methyltransferase [HGNC gene]
- MTR Gene [NCIt concept]
- MTR gene [LOINC component]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients