Phosphate cytidylyltransferase 2, ethanolamine

Preferred Label : Phosphate cytidylyltransferase 2, ethanolamine;

Symbol : PCYT2;

CISMeF acronym : PCYT2;

Type : Gene;

Alternative titles and symbols : Cytidylyltransferase, ctp-phosphoethanolamine; Ethanolamine-phosphate cytidylyltransferase; ET;

Ensembl ID : ENSG00000185813;

Prefixed ID : *602679;

Details

Origin ID

602679;

UMLS CUI

C1418398;

Automatic exact mappings (from CISMeF team)
- Contact with health services for embryo transfer [ICD-11 Sub-sub category]
- Disorders of Eustachian tube [ICD-11 Category]
- Endotracheal Route of Administration [NCIt concept]
- Essential Thrombocythemia [NCIt concept]
- Essential thrombocythemia [ORDO Disease]
- Ethanolamine-phosphate cytidylyltransferase [MeSH concept]
- Ethanolamine-phosphate cytidylyltransferase (substance) [SNOMED CT concept]
- ethanolamine-phosphate cytidylyltransferase [SNOMED Notion]
- ethanolamine-phosphate cytidylyltransferase [MeSH Supplementary Concept]
- ethanolamine-phosphate cytidylyltransferase activity [GO term]
- phosphate cytidylyltransferase 2, ethanolamine [HGNC gene]
False automatic mappings
- Docetaxel/Epirubicin Regimen [NCIt concept]
- Ethiopia [NCIt concept]
HGNC gene
- phosphate cytidylyltransferase 2, ethanolamine [HGNC gene]
ORDO concept(s)
- phosphate cytidylyltransferase 2, ethanolamine [ORDO Gene]
Phenotypes related
- Spastic paraplegia 82, autosomal recessive [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- phosphate cytidylyltransferase 2, ethanolamine [HGNC gene]

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