OMOP Concept 36716398
Congenital lethal erythroderma
StandardConditionSNOMED722391005Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Congenital lethal erythroderma via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535513 | Lethal congenital erythroderma | Non-standard |
| Nebraska Lexicon | 722391005 | Congenital lethal erythroderma | Non-standard |
Synonyms
Alternative names recorded for Congenital lethal erythroderma across source vocabularies.
- Congenital lethal erythroderma (disorder)
- eritrodermia congénita letal
- eritrodermia congénita letal (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(34)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital disease
- 1Disorder involving the integument of fetus OR newborn
- 1Erythroderma
- 1Hereditary disorder of the integument
- 1Inflammatory dermatosis
- 2Autosomal hereditary disorder
- 2Disorder of fetus and/or newborn
- 2Disorder of integument
- 2Disorder of skin
- 2Erythema of skin
- 2Hereditary disorder by system
- 2Inflammation of skin and/or subcutaneous tissue
- 2Inflammation of specific body organs
- 3Disease
- 3Disorder of body system
- 3Disorder of skin and/or subcutaneous tissue
- 3Eruption
- 3Erythema
- 3Hereditary disease
- 3Inflammation of specific body structures or tissue
- 3Inflammation of specific body systems
- 3Integumentary system finding
- 3Skin finding
- 4Clinical finding
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