glyoxylate and hydroxypyruvate reductase

Preferred Label : glyoxylate and hydroxypyruvate reductase;

Approved symbol HGNC : GRHPR;

Name synonyms HGNC : primary hyperoxaluria type 2;

Alias symbols HGNC : PH2;

Chromosome HGNC : 9p13.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000137106;

Details

Origin ID

HGNC:4570;

UMLS CUI

C1415286;

Automatic exact mappings (from CISMeF team)
- Glyoxylate reductase/hydroxypyruvate reductase [OMIM gene]
- Primary hyperoxaluria type 2 [ICD-11 More detail]
- Primary hyperoxaluria type 2 [ORDO Disease]
- Primary hyperoxaluria type 2 [MeSH concept]
- glyoxylate and hydroxypyruvate reductase [ORDO Gene]
- primary hyperoxaluria type 2 [MeSH Supplementary Concept]
- primary hyperoxaluria type 2 [DO Concept]
NCIt concept
- GRHPR Gene [NCIt concept]
OMIM gene
- Glyoxylate reductase/hydroxypyruvate reductase [OMIM gene]
Orphanet gene
- glyoxylate and hydroxypyruvate reductase [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- GRHPR Gene [NCIt concept]
- GRHPR gene [LOINC component]
- Glyoxylate reductase/hydroxypyruvate reductase [OMIM gene]

Keyword's position in hierarchy(ies) :

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