Phosphoserine phosphatase

Preferred Label : Phosphoserine phosphatase;

Symbol : PSPH;

CISMeF acronym : PSPH;

Type : Gene;

Alternative titles and symbols : PSP;

Ensembl ID : ENSG00000146733;

Prefixed ID : *172480;

Details

Origin ID

172480;

UMLS CUI

C1419048;

Automatic exact mappings (from CISMeF team)
- CHGA wt Allele [NCIt concept]
- Chromogranin-A [NCIt concept]
- Lithostathine-1-Alpha [NCIt concept]
- MSMB wt Allele [NCIt concept]
- PSPN wt Allele [NCIt concept]
- Persephin [NCIt concept]
- Phosphoserine phosphatase (substance) [SNOMED CT concept]
- Progressive supranuclear ophthalmoplegia (disorder) [SNOMED CT concept]
- REG1A wt Allele [NCIt concept]
- Regenerating islet-derived 1 alpha (pancreatic stone protein, pancreatic thread protein) [ORDO Gene]
- microseminoprotein beta [ORDO Gene]
- phosphoserine phosphatase [ORDO Gene]
- phosphoserine phosphatase [MeSH concept]
- phosphoserine phosphatase [MeSH Supplementary Concept]
- phosphoserine phosphatase [HGNC gene]
- phosphoserine phosphatase [SNOMED Notion]
- progressive supranuclear palsy [MedlinePlus Topic]
HGNC gene
- phosphoserine phosphatase [HGNC gene]
ORDO concept(s)
- phosphoserine phosphatase [ORDO Gene]
Phenotypes related
- Phosphoserine phosphatase deficiency [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- phosphoserine phosphatase [HGNC gene]

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