cytidine deaminase

Preferred Label : cytidine deaminase;

Approved symbol HGNC : CDA;

Alias symbols HGNC : CDD;

Chromosome HGNC : 1p36.12;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000158825;

Details

Origin ID

HGNC:1712;

UMLS CUI

C1413247;

Automatic exact mappings (from CISMeF team)
- Corneal dystrophy, avellino type [OMIM Phenotype]
- Craniodiaphyseal dysplasia [OMIM Phenotype]
- Craniodiaphyseal dysplasia, autosomal dominant [OMIM Phenotype]
- Cytidine Deaminase [NCIt concept]
- Cytidine deaminase [OMIM gene]
- Cytidine deaminase (substance) [SNOMED CT concept]
- cytidine deaminase [SNOMED Notion]
- cytidine deaminase [MeSH Descriptor]
- cytidine deaminase [MeSH concept]
NCIt concept
- CDA Gene [NCIt concept]
OMIM gene
- Cytidine deaminase [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CDA Gene [NCIt concept]
- Cytidine deaminase [OMIM gene]

Keyword's position in hierarchy(ies) :

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