Keratitis – ichthyosis – deafness syndrome

Preferred Label : Keratitis – ichthyosis – deafness syndrome;

ICD-11 definition : Keratitis (and hystrix-like) ichthyosis deafness (KID/HID) syndrome is a rare congenital ectodermal disorder characterized by vascularizing keratitis, hyperkeratotic skin lesions and hearing loss.;

ICD-11 synonym : KID/HID syndrome; KID - [Keratitis – ichthyosis – deafness syndrome] syndrome; KID/HID - [Keratitis - ichthyosis - deafness/Hystrix-like ichthyosis - deafness] syndrome; Hystrix-like ichthyosis - deafness; Keratitis - ichthyosis - deafness/Hystrix-like ichthyosis - deafness; KID syndrome; Senter syndrome;

Details

Origin ID

1152535279;

Automatic exact mappings (from CISMeF team)
- HID syndrome [MeSH Supplementary Concept]
- Ichthyosis, hystrix-like, with deafness [OMIM Phenotype]
Currated CISMeF NLP mapping
- KID syndrome [ORDO Disease]
- KID syndrome [PASCAL descriptor]
- Keratitis ichthyosis and deafness syndrome (disorder) [SNOMED CT concept]
- Keratitis, Ichthyosis, and Deafness (KID) Syndrome [MeSH concept]
- Keratitis-Ichthyosis-Deafness syndrome [MeSH concept]
- Keratitis-Ichthyosis-Deafness syndrome [MeSH Supplementary Concept]
- 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.)]
- keratitis, ichthyosis, and deafness (KID) syndrome [MeSH Supplementary Concept]
- senter syndrome [SNOMED Notion]

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