Tubulin-specific chaperone D

Preferred Label : Tubulin-specific chaperone D;

Symbol : TBCD;

CISMeF acronym : TBCD;

Type : Gene;

Ensembl ID : ENSG00000141556;

Prefixed ID : *604649;

Details

Origin ID

604649;

UMLS CUI

C1420596;

Automatic exact mappings (from CISMeF team)
- Thiel-Behnke corneal dystrophy [ORDO Disease]
- Thiel-Behnke corneal dystrophy [DO Concept]
- tubulin folding cofactor D [HGNC gene]
- tubulin folding cofactor D [ORDO Gene]
HGNC gene
- tubulin folding cofactor D [HGNC gene]
ORDO concept(s)
- tubulin folding cofactor D [ORDO Gene]
Phenotypes related
- Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- tubulin folding cofactor D [HGNC gene]

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