keratitis, ichthyosis, and deafness (KID) syndrome

Preferred Label : keratitis, ichthyosis, and deafness (KID) syndrome;

MeSH synonym : keratitis-ichthyosis-deafness syndrome, autosomal dominant; KID syndrome; kid syndrome, autosomal dominant;

Détails

Origin ID

C536168;

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]
MeSH term(s) associated for indexing
- deafness [MeSH Descriptor]
- ichthyosis [MeSH Descriptor]
- keratitis [MeSH Descriptor]
Record concept(s)
- Keratitis, Ichthyosis, and Deafness (KID) Syndrome [MeSH concept]
See also (suggested by CISMeF)
- ichthyosiform erythroderma, corneal involvement, deafness [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]

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