OFD1 centriole and centriolar satellite protein

Preferred Label : OFD1 centriole and centriolar satellite protein;

Approved symbol HGNC : OFD1;

Name synonyms HGNC : Joubert syndrome type 10;

Alias symbols HGNC : 71-7A; JBTS10;

Chromosome HGNC : Xp22.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000046651;

Détails

Origin ID

HGNC:2567;

UMLS CUI

C1413833;

Automatic exact mappings (from CISMeF team)
- Joubert syndrome 10 [OMIM Phenotype]
- OFD1 centriole and centriolar satellite protein [ORDO Gene]
- Ofd1 centriole and centriolar satellite protein [OMIM gene]
- Orofaciodigital syndrome I [OMIM Phenotype]
NCIt concept
- OFD1 Gene [NCIt concept]
OMIM gene
- Ofd1 centriole and centriolar satellite protein [OMIM gene]
Orphanet gene
- OFD1 centriole and centriolar satellite protein [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- OFD1 Gene [NCIt concept]
- Ofd1 centriole and centriolar satellite protein [OMIM gene]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients