Keratitis, Ichthyosis, and Deafness (KID) Syndrome

Preferred Label : Keratitis, Ichthyosis, and Deafness (KID) Syndrome;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0530629;

UMLS CUI

C0265336;

Currated CISMeF NLP mapping
- KID syndrome [PASCAL descriptor]
- KID syndrome [ORDO Disease]
- Keratitis ichthyosis and deafness syndrome (disorder) [SNOMED CT concept]
- Keratitis – ichthyosis – deafness syndrome [ICD-11 More detail]
- Keratitis-ichthyosis-deafness syndrome [MedDRA Preferred Term]
- Keratitis-ichthyosis-deafness syndrome, autosomal dominant [OMIM Phenotype]
- Senter syndrome (disorder) [SNOMED CT concept]
- autosomal dominant keratitis-ichthyosis-deafness syndrome [DO Concept]
- keratitis ichthyosis deafness syndrome [Disease (Nov.)]
- senter syndrome [SNOMED Notion]
Related record
- keratitis, ichthyosis, and deafness (KID) syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- KID syndrome [ORDO Disease]
- Keratitis-ichthyosis-deafness syndrome, autosomal dominant [OMIM Phenotype]
- Senter syndrome (disorder) [SNOMED CT concept]
- senter syndrome [SNOMED Notion]