keratin 10 - CISMeF

Preferred Label : keratin 10;

Approved symbol HGNC : KRT10;

Name synonyms HGNC : epidermolytic hyperkeratosis; cytokeratin 10;

Alias symbols HGNC : CK10; K10;

Chromosome HGNC : 17q21.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000186395;

Details

Origin ID

HGNC:6413;

UMLS CUI

C1416714;

Automatic exact mappings (from CISMeF team)
- Autosomal dominant epidermolytic ichthyosis [ORDO Disease]
- Bullous ichthyosiform erythroderma (disorder) [SNOMED CT concept]
- Congenital bullous ichthyosiform erythroderma [HPO term]
- Epidermolytic Ichthyosis [NCIt concept]
- Epidermolytic hyperkeratosis [MedDRA LLT]
- Epidermolytic hyperkeratosis [PASCAL descriptor]
- Epidermolytic hyperkeratosis 1 [OMIM Phenotype]
- Epidermolytic ichthyosis [ICD-11 More detail]
- Keratin 10, type I [OMIM gene]
- Keratin, Type I Cytoskeletal 10 [NCIt concept]
- Keratin-10 [MeSH Descriptor]
- epidermolytic hyperkeratosis [DO Concept]
- hyperkeratosis, epidermolytic [MeSH Descriptor]
- hyperkeratosis, epidermolytic [MeSH concept]
- keratin 10 [ORDO Gene]
NCIt concept
- KRT10 Gene [NCIt concept]
OMIM gene
- Keratin 10, type I [OMIM gene]
Orphanet gene
- keratin 10 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- KRT10 Gene [NCIt concept]
- Keratin 10, type I [OMIM gene]

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