OMOP Concept 4286173
Congenital keratoderma
StandardConditionSNOMED6874009Disorder
Maps from
3
Descendants
4
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to Congenital keratoderma via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 143875 | Congenital Keratoderma | Non-standard |
| Nebraska Lexicon | 6874009 | Congenital keratoderma | Non-standard |
| Read | PH3y300 | Congenital keratoderma | Non-standard |
Synonyms
Alternative names recorded for Congenital keratoderma across source vocabularies.
- Congenital keratoderma (disorder)
- queratoderma congénita
- queratodermia congénita
- queratodermia congénita (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(26)Roll up to these when you need a wider cohort.
- 1Congenital disease
- 1Disorder involving the integument of fetus OR newborn
- 1Erythrokeratoderma
- 1Keratoderma
- 1Rough skin
- 2Abnormal keratinization
- 2Disorder of fetus and/or newborn
- 2Disorder of integument
- 2Disorder of skin
- 2Inherited disorder of keratinization
- 2Keratosis
- 2Skin finding
- 3Disease
- 3Disorder of body system
- 3Disorder of keratinization
- 3Disorder of skin and/or subcutaneous tissue
- 3Functional finding
- 3General finding of soft tissue
- 3Hereditary disorder of the integument
- 3Integumentary system finding
- 3Skin AND/OR mucosa finding
- 4Clinical finding
- 4Disorder of soft tissue
- 4Hereditary disorder by system
- 5Hereditary disease
Narrower concepts
(4)Included automatically when you query with descendants.
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