Nhp2 ribonucleoprotein

Preferred Label : Nhp2 ribonucleoprotein;

Symbol : NHP2;

CISMeF acronym : NOLA2;

Type : Gene;

Alternative titles and symbols : Nhp2, s. cerevisiae, homolog of; Nucleolar protein family a, member 2; NOLA2;

Ensembl ID : ENSG00000145912;

Prefixed ID : *606470;

Details

Origin ID

606470;

UMLS CUI

C1422601;

Automatic exact mappings (from CISMeF team)
- H/ACA Ribonucleoprotein Complex Subunit 2 [NCIt concept]
- NHP2 Gene [NCIt concept]
- NHP2 ribonucleoprotein [HGNC gene]
- NHP2 ribonucleoprotein [ORDO Gene]
- NHP2 wt Allele [NCIt concept]
HGNC gene
- NHP2 ribonucleoprotein [HGNC gene]
NCIt concept(s)
- H/ACA Ribonucleoprotein Complex Subunit 2 [NCIt concept]
- NHP2 Gene [NCIt concept]
- NHP2 wt Allele [NCIt concept]
ORDO concept(s)
- NHP2 ribonucleoprotein [ORDO Gene]
Phenotypes related
- Dyskeratosis congenita, autosomal recessive 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NHP2 Gene [NCIt concept]
- NHP2 ribonucleoprotein [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients