OMOP Concept 4295600
Autosomal recessive keratitis-ichthyosis-deafness syndrome
StandardConditionSNOMED403780007Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal recessive keratitis-ichthyosis-deafness syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537363 | Ichthyosiform erythroderma, corneal involvement, deafness | Non-standard |
Synonyms
Alternative names recorded for Autosomal recessive keratitis-ichthyosis-deafness syndrome across source vocabularies.
- Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder)
- Autosomal recessive KID (keratitis, ichthyosis, deafness) syndrome
- síndrome autosómico recesivo de queratitis-ictiosis-sordera
- síndrome autosómico recesivo de queratitis-ictiosis-sordera (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(52)Roll up to these when you need a wider cohort.
- 1Autosomal recessive ichthyosis
- 1KID syndrome
- 2Autosomal recessive hereditary disorder
- 2Congenital hearing disorder
- 2Congenital ichthyosis of skin
- 2Cutaneous syndrome with ichthyosis
- 2Decreased hearing
- 2Ectodermal dysplasia
- 2Hearing loss associated with syndrome
- 2Hereditary hearing loss
- 3Auditory system hereditary disorder
- 3Autosomal hereditary disorder
- 3Congenital disease
- 3Congenital ectodermal defect
- 3Decline in functional status
- 3Developmental hereditary disorder
- 3Genodermatosis
- 3Hearing disorder
- 3Hearing finding
- 3Hearing loss
- 3Hereditary disorder of the integument
- 3Ichthyosis
- 3Inherited disorder of keratinization
- 3Rough skin
- 4Abnormal keratinization
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