ribosomal protein S19

Preferred Label : ribosomal protein S19;

Approved symbol HGNC : RPS19;

Name synonyms HGNC : Diamond-Blackfan anemia;

Alias symbols HGNC : DBA; eS19; S19;

Chromosome HGNC : 19q13.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000105372;

Details

Origin ID

HGNC:10402;

UMLS CUI

C1335641;

Automatic exact mappings (from CISMeF team)
- 40S Ribosomal Protein S19 [NCIt concept]
- Blackfan-Diamond anemia [ORDO Disease]
- Congenital Pure Red Cell Aplasia [NCIt concept]
- Congenital hypoplastic anemia (disorder) [SNOMED CT concept]
- Diamond-Blackfan anemia [DO Concept]
- Diamond-Blackfan anemia [MedDRA LLT]
- Ribosomal protein s19 [OMIM gene]
- anemia, Diamond-Blackfan [MeSH concept]
- anemia, diamond-blackfan [MeSH Descriptor]
- ribosomal protein S19 [ORDO Gene]
- ribosomal protein S19 [MeSH Supplementary Concept]
- ribosomal protein S19 [MeSH concept]
NCIt concept
- RPS19 Gene [NCIt concept]
OMIM gene
- Ribosomal protein s19 [OMIM gene]
Orphanet gene
- ribosomal protein S19 [ORDO Gene]
See also inter- (CISMeF)
- Diamond-blackfan anemia [OMIM phenotypic series]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- RPS19 Gene [NCIt concept]
- RPS19 gene [LOINC component]
- Ribosomal protein s19 [OMIM gene]

Keyword's position in hierarchy(ies) :

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