Ofd1 centriole and centriolar satellite protein

Preferred Label : Ofd1 centriole and centriolar satellite protein;

Symbol : OFD1;

CISMeF acronym : OFD1;

Type : Gene;

Alternative titles and symbols : Ofd1 gene; Chromosome X open reading frame 5; CXORF5;

Ensembl ID : ENSG00000046651;

Prefixed ID : *300170;

Details

Origin ID

300170;

UMLS CUI

C1413833;

Automatic exact mappings (from CISMeF team)
- OFD1 Gene [NCIt concept]
- OFD1 centriole and centriolar satellite protein [ORDO Gene]
- OFD1 centriole and centriolar satellite protein [HGNC gene]
- OFD1 wt Allele [NCIt concept]
- Oral-facial-digital syndrome type 1 [ICD-11 More detail]
- Orofaciodigital syndrome type 1 [ORDO Disease]
HGNC gene
- OFD1 centriole and centriolar satellite protein [HGNC gene]
NCIt concept(s)
- OFD1 Gene [NCIt concept]
- OFD1 wt Allele [NCIt concept]
- Oral-Facial-Digital Syndrome 1 Protein [NCIt concept]
ORDO concept(s)
- OFD1 centriole and centriolar satellite protein [ORDO Gene]
Phenotypes related
- Joubert syndrome 10 [OMIM Phenotype]
- Orofaciodigital syndrome I [OMIM Phenotype]
- Retinitis pigmentosa 23 [OMIM Phenotype]
- Simpson-golabi-behmel syndrome, type 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- OFD1 Gene [NCIt concept]
- OFD1 centriole and centriolar satellite protein [HGNC gene]

Keyword's position in hierarchy(ies) :

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