Carbamoyl phosphate synthetase/aspartate transcarbamylase/dihydroorotase

Preferred Label : Carbamoyl phosphate synthetase/aspartate transcarbamylase/dihydroorotase;

Symbol : CAD;

CISMeF acronym : CAD;

Type : Gene;

Alternative titles and symbols : Cad trifunctional protein; CPSase/ATCase/DHOase;

Ensembl ID : ENSG00000084774;

Prefixed ID : *114010;

Details

Origin ID

114010;

UMLS CUI

C1413078;

Automatic exact mappings (from CISMeF team)
- CAD Gene [NCIt concept]
- CALD1 wt Allele [NCIt concept]
- Caddo Language [NCIt concept]
- Cold agglutinin disease [ORDO Disease]
- Collision-Induced Dissociation [NCIt concept]
- Computer aided design [UNESCO concept]
- Computer-Aided Diagnosis [NCIt concept]
- Coronary Artery Disease [NCIt concept]
- Coronary atherosclerosis [ICD-11 Category]
- DFFB wt Allele [NCIt concept]
- DNA Fragmentation Factor Subunit Beta [NCIt concept]
- DNA fragmentation factor subunit beta [HGNC gene]
- Family History of Coronary Artery Disease [NCIt concept]
- aconitate decarboxylase 1 [HGNC gene]
- carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase [HGNC gene]
- carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase [ORDO Gene]
- computer-aided design [MeSH Descriptor]
- coronary artery disease [MedlinePlus Topic]
- diagnosis, computer-assisted [MeSH Descriptor]
HGNC gene
- carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase [HGNC gene]
NCIt concept(s)
- CAD Gene [NCIt concept]
- CAD Protein [NCIt concept]
- CAD wt Allele [NCIt concept]
ORDO concept(s)
- carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase [ORDO Gene]
Phenotypes related
- Developmental and epileptic encephalopathy 50 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CAD Gene [NCIt concept]
- carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase [HGNC gene]

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