OMOP Concept 37110883
Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type
StandardConditionSNOMED725407006Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 725407006 | RDEB-O - recessive dystrophic epidermolysis bullosa-generalised other | Non-standard |
Synonyms
Alternative names recorded for Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type across source vocabularies.
- epidermólisis bullosa distrófica recesiva no tipo Hallopeau-Siemens
- epidermólisis bullosa distrófica recesiva no tipo Hallopeau-Siemens (trastorno)
- RDEB-O - recessive dystrophic epidermolysis bullosa-generalised other
- RDEB-O - recessive dystrophic epidermolysis bullosa-generalized other
- Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(32)Roll up to these when you need a wider cohort.
- 1Generalized dystrophic epidermolysis bullosa
- 1Recessive dystrophic epidermolysis bullosa
- 2Autosomal recessive hereditary disorder
- 2Dystrophic epidermolysis bullosa
- 3Autosomal hereditary disorder
- 3Epidermolysis bullosa
- 4Degenerative skin disorder
- 4Developmental hereditary disorder
- 4Genodermatosis
- 4Hereditary disease
- 4Hereditary disorder of the integument
- 5Congenital anomaly of skin
- 5Degenerative disorder
- 5Developmental disorder
- 5Disorder of integument
- 5Disorder of skin
- 5Genetic disease
- 5Hereditary disorder by system
- 6Congenital anomaly of integument
- 6Disease
- 6Disorder of body system
- 6Disorder of skin and/or subcutaneous tissue
- 6Integumentary system finding
- 6Skin finding
- 7Clinical finding
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