keratosis linearis with ichthyosis congenita and sclerosing keratoderma

Preferred Label : keratosis linearis with ichthyosis congenita and sclerosing keratoderma;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0566900;

UMLS CUI

C1866029;

Currated CISMeF NLP mapping
- Keratosis linearis with ichthyosis congenita and sclerosing keratoderma [OMIM Phenotype]
- Keratosis linearis – ichthyosis congenita – keratoderma [ICD-11 More detail]
- Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome (disorder) [SNOMED CT concept]
- Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome [ORDO Disease]
Related record
- keratosis linearis with ichthyosis congenita and sclerosing keratoderma [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Keratosis linearis with ichthyosis congenita and sclerosing keratoderma [OMIM Phenotype]
- Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome (disorder) [SNOMED CT concept]
- Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome [ORDO Disease]