SLX4 structure-specific endonuclease subunit

Preferred Label : SLX4 structure-specific endonuclease subunit;

Approved symbol HGNC : SLX4;

Name synonyms HGNC : Fanconi anemia; complementation group P;

Alias symbols HGNC : KIAA1987; KIAA1784; FANCP;

Chromosome HGNC : 16p13.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000188827;

Details

Origin ID

HGNC:23845;

UMLS CUI

C1428293;

Automatic exact mappings (from CISMeF team)
- Fanconi Anemia [NCIt concept]
- Fanconi anemia [PASCAL descriptor]
- Fanconi anemia [ORDO Disease]
- Fanconi anemia [DO Concept]
- Fanconi anemia [OMIM phenotypic series]
- Fanconi anemia, complementation group a [OMIM Phenotype]
- Fanconi anemia, complementation group p [OMIM Phenotype]
- Fanconi's anemia [MedDRA LLT]
- Fanconi's anemia (disorder) [SNOMED CT concept]
- SLX4 structure-specific endonuclease subunit [ORDO Gene]
- Slx4 structure-specific endonuclease subunit [OMIM gene]
- Structure-Specific Endonuclease Subunit SLX4 [NCIt concept]
- aplastic anemia [MedlinePlus Topic]
- fanconi anemia [MeSH Descriptor]
- fanconi anemia [MeSH concept]
NCIt concept
- SLX4 Gene [NCIt concept]
OMIM gene
- Slx4 structure-specific endonuclease subunit [OMIM gene]
Orphanet gene
- SLX4 structure-specific endonuclease subunit [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLX4 Gene [NCIt concept]
- Slx4 structure-specific endonuclease subunit [OMIM gene]

Keyword's position in hierarchy(ies) :

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