keratin 12 - CISMeF

Preferred Label : keratin 12;

Approved symbol HGNC : KRT12;

Name synonyms HGNC : Meesmann corneal dystrophy;

Alias symbols HGNC : K12;

Chromosome HGNC : 17q21.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000187242;

Details

Origin ID

HGNC:6414;

UMLS CUI

C1416715;

Automatic exact mappings (from CISMeF team)
- Keratin, Type I Cytoskeletal 12 [NCIt concept]
- Keratin-12 [MeSH Descriptor]
- Meesmann Corneal Dystrophy [NCIt concept]
- Meesmann corneal dystrophy [DO Concept]
- Meesmann corneal dystrophy [PASCAL descriptor]
- Meesmann corneal dystrophy [ORDO Disease]
- corneal dystrophy, juvenile epithelial of meesmann [MeSH Descriptor]
Currated CISMeF NLP mapping
- KRT12 Gene [NCIt concept]
- Keratin 12, type I [OMIM gene]
- keratin 12 [ORDO Gene]
NCIt concept
- KRT12 Gene [NCIt concept]
OMIM gene
- Keratin 12, type I [OMIM gene]
Orphanet gene
- keratin 12 [ORDO Gene]
See also inter- (CISMeF)
- Corneal dystrophy, meesmann [OMIM phenotypic series]
- 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, type I [OMIM gene]

Keyword's position in hierarchy(ies) :

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