Keratin 12, type I - CISMeF

" /> Keratin 12, type I - CISMeF

CISMeF

chu

Keratin 12, type IOMIM gene

Preferred Label : Keratin 12, type I;

Symbol : KRT12;

CISMeF acronym : KRT12;

Type : Gene;

Alternative titles and symbols : Cytokeratin 12; K12; KA12;

Ensembl ID : ENSG00000187242;

Prefixed ID : *601687;

Details

Origin ID

601687;

UMLS CUI

C1416715;

Automatic exact mappings (from CISMeF team)
- Keratin, Type I Cytoskeletal 12 [NCIt concept]
- Keratin-12 [MeSH Descriptor]
- SECTM1 wt Allele [NCIt concept]
Currated CISMeF NLP mapping
- KRT12 Gene [NCIt concept]
- KRT12 wt Allele [NCIt concept]
- keratin 12 [ORDO Gene]
- keratin 12 [HGNC gene]
HGNC gene
- keratin 12 [HGNC gene]
NCIt concept(s)
- KRT12 Gene [NCIt concept]
- KRT12 wt Allele [NCIt concept]
- Keratin, Type I Cytoskeletal 12 [NCIt concept]
ORDO concept(s)
- keratin 12 [ORDO Gene]
Phenotypes related
- Corneal dystrophy, meesmann, 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- KRT12 Gene [NCIt concept]
- keratin 12 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
16/05/2024

© Rouen University Hospital. Any partial or total use of this material must mention the source.

" /> Keratin 12, type I - CISMeF

CISMeF

chu

Keratin 12, type IOMIM gene

Preferred Label : Keratin 12, type I;

Symbol : KRT12;

CISMeF acronym : KRT12;

Type : Gene;

Alternative titles and symbols : Cytokeratin 12; K12; KA12;

Ensembl ID : ENSG00000187242;

Prefixed ID : *601687;

Details

Origin ID

601687;

UMLS CUI

C1416715;

Automatic exact mappings (from CISMeF team)
- Keratin, Type I Cytoskeletal 12 [NCIt concept]
- Keratin-12 [MeSH Descriptor]
- SECTM1 wt Allele [NCIt concept]
Currated CISMeF NLP mapping
- KRT12 Gene [NCIt concept]
- KRT12 wt Allele [NCIt concept]
- keratin 12 [ORDO Gene]
- keratin 12 [HGNC gene]
HGNC gene
- keratin 12 [HGNC gene]
NCIt concept(s)
- KRT12 Gene [NCIt concept]
- KRT12 wt Allele [NCIt concept]
- Keratin, Type I Cytoskeletal 12 [NCIt concept]
ORDO concept(s)
- keratin 12 [ORDO Gene]
Phenotypes related
- Corneal dystrophy, meesmann, 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- KRT12 Gene [NCIt concept]
- keratin 12 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
16/05/2024

© Rouen University Hospital. Any partial or total use of this material must mention the source.