Neurochondrin - CISMeF

Preferred Label : Neurochondrin;

Symbol : NCDN;

CISMeF acronym : NCDN;

Type : Gene;

Alternative titles and symbols : NORBIN; KIAA0607;

Ensembl ID : ENSG00000020129;

Prefixed ID : *608458;

Details

Origin ID

608458;

UMLS CUI

C1538048;

Automatic exact mappings (from CISMeF team)
- neurochondrin [HGNC gene]
- neurochondrin [MeSH concept]
- neurochondrin [MeSH Supplementary Concept]
- norbin [MeSH Supplementary Concept]
- norbin [MeSH concept]
HGNC gene
- neurochondrin [HGNC gene]
ORDO concept(s)
- neurochondrin [ORDO Gene]
Phenotypes related
- Neurodevelopmental disorder with infantile epileptic spasms [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- neurochondrin [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients