Nme/nm23 family, member 8

Preferred Label : Nme/nm23 family, member 8;

Symbol : NME8;

CISMeF acronym : NME8;

Type : Gene;

Alternative titles and symbols : Thioredoxin domain-containing protein 3; Sperm-specific thioredoxin 2; TXNDC3; SPTRX2;

Ensembl ID : ENSG00000086288;

Prefixed ID : *607421;

Détails

Origin ID

607421;

UMLS CUI

C1424308;

Automatic exact mappings (from CISMeF team)
- NME/NM23 family member 8 [ORDO Gene]
- NME/NM23 family member 8 [HGNC gene]
HGNC gene
- NME/NM23 family member 8 [HGNC gene]
ORDO concept(s)
- NME/NM23 family member 8 [ORDO Gene]
Phenotypes related
- Ciliary dyskinesia, primary, 6 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NME/NM23 family member 8 [HGNC gene]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients