Paired-like homeobox 2b

Preferred Label : Paired-like homeobox 2b;

Symbol : PHOX2B;

CISMeF acronym : PHOX2B;

Type : Gene;

Alternative titles and symbols : Paired mesoderm homeobox 2b; Neuroblastoma paired-type homeobox gene; PMX2B; NBPHOX;

Ensembl ID : ENSG00000109132;

Prefixed ID : *603851;

Details

Origin ID

603851;

UMLS CUI

C1418697;

Automatic exact mappings (from CISMeF team)
- NBPhox protein [MeSH Supplementary Concept]
- PHOX2B Gene [NCIt concept]
- PHOX2B gene [LOINC component]
- PHOX2B wt Allele [NCIt concept]
- Paired Mesoderm Homeobox Protein 2B [NCIt concept]
- paired like homeobox 2B [ORDO Gene]
- paired like homeobox 2B [HGNC gene]
HGNC gene
- paired like homeobox 2B [HGNC gene]
NCIt concept(s)
- PHOX2B Gene [NCIt concept]
- PHOX2B wt Allele [NCIt concept]
- Paired Mesoderm Homeobox Protein 2B [NCIt concept]
ORDO concept(s)
- paired like homeobox 2B [ORDO Gene]
Phenotypes related
- Central hypoventilation syndrome, congenital, 1 [OMIM Phenotype]
- Neuroblastoma, susceptibility to, 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PHOX2B Gene [NCIt concept]
- PHOX2B gene [LOINC component]
- paired like homeobox 2B [HGNC gene]

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