OMOP Concept 37116373
Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome
StandardConditionSNOMED733064004Disorder
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 Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537138 | Oslam syndrome | Non-standard |
Synonyms
Alternative names recorded for Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome across source vocabularies.
- OSLAM (osteosarcoma, limb anomalies, erythroid macrocytosis) syndrome
- OSLAM syndrome
- Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome (disorder)
- síndrome de osteosarcoma, anomalías de los miembros y macrocitosis eritroide
- síndrome de osteosarcoma, anomalías de los miembros y macrocitosis eritroide (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(48)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital anomaly of limb
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Hereditary red blood cell disorder
- 1Macrocytosis - no anemia
- 1Multiple malformation syndrome with limb defect as major feature
- 1Osteosarcoma of bone
- 2Autosomal hereditary disorder
- 2Congenital malformation
- 2Developmental disorder
- 2Disorder of limb
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hereditary disorder of cellular element of blood
- 2Multiple system malformation syndrome
- 2Non-anemic red cell disorder
- 2Osteosarcoma
- 2Red blood cell disorder
- 2Sarcoma of bone
- 3Congenital disease
- 3Congenital malformation syndrome
- 3Disease
- 3Disorder of body system
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