Noggin - CISMeF

Preferred Label : Noggin;

Symbol : NOG;

CISMeF acronym : NOG;

Type : Gene;

Alternative titles and symbols : Noggin, mouse, homolog of;

Ensembl ID : ENSG00000183691;

Prefixed ID : *602991;

Details

Origin ID

602991;

UMLS CUI

C1417753;

Automatic exact mappings (from CISMeF team)
- Nogai Language [NCIt concept]
- gill [UCUM unit]
- noggin [ORDO Gene]
- noggin [HGNC gene]
HGNC gene
- noggin [HGNC gene]
ORDO concept(s)
- noggin [ORDO Gene]
Phenotypes related
- Brachydactyly, type b2 [OMIM Phenotype]
- Multiple synostoses syndrome 1 [OMIM Phenotype]
- Stapes ankylosis with broad thumbs and toes [OMIM Phenotype]
- Symphalangism, proximal, 1a [OMIM Phenotype]
- Tarsal-carpal coalition syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- noggin [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients