OMOP Concept 36676721
Sterile multifocal osteomyelitis with periostitis and pustulosis
StandardConditionSNOMED773702002Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2019
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Sterile multifocal osteomyelitis with periostitis and pustulosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C557815 | Deficiency of interleukin-1 receptor antagonist | Non-standard |
Synonyms
Alternative names recorded for Sterile multifocal osteomyelitis with periostitis and pustulosis across source vocabularies.
- Autoinflammatory disease due to interleukin-1 receptor antagonist deficiency
- Interleukin-1 receptor antagonist deficiency
- OMPP - sterile osteomyelitis, multifocal with periostitis and pustulosis
- osteomielitis multifocal estéril con periostitis y pustulosis
- osteomielitis multifocal estéril con periostitis y pustulosis (trastorno)
- Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(56)Roll up to these when you need a wider cohort.
- 1Autoinflammatory disease
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of skeletal bone
- 1Congenital immunodeficiency disease
- 1Developmental hereditary disorder
- 1Hereditary disorder of immune system
- 1Hereditary disorder of musculoskeletal system
- 1Hereditary disorder of the integument
- 1Lesion of bone
- 1Neonatal dermatosis
- 1Primary immune deficiency disorder
- 1Pustule
- 1Skeletal dysplasia
- 2Autosomal hereditary disorder
- 2Congenital anomaly of musculoskeletal system
- 2Congenital disease
- 2Dermatosis of infancy
- 2Developmental disorder
- 2Disorder of bone
- 2Disorder of bone development
- 2Disorder of immune function
- 2Disorder of integument
- 2Disorder of musculoskeletal system
- 2Disorder of skin
- 2Fetal and/or neonatal disorder of integument
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