OMOP Concept 36676403
Familial osteodysplasia Anderson type
StandardConditionSNOMED773278003Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2019
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Familial osteodysplasia Anderson type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C564923 | Osteodysplasia, Familial, Anderson Type | Non-standard |
Synonyms
Alternative names recorded for Familial osteodysplasia Anderson type across source vocabularies.
- Familial osteodysplasia Anderson type (disorder)
- osteodisplasia familiar tipo Anderson
- osteodisplasia familiar tipo Anderson (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(36)Roll up to these when you need a wider cohort.
- 1Congenital abnormality of skull and face bones
- 1Familial disease
- 1Lesion of bone
- 1Lesion of face
- 1Skeletal dysplasia
- 2Congenital anomaly of face bones
- 2Congenital anomaly of musculoskeletal system
- 2Congenital anomaly of skull
- 2Disease
- 2Disorder of bone
- 2Disorder of face
- 2Structural abnormality of skeleton
- 3Bone finding
- 3Clinical finding
- 3Congenital anomaly of bone of head
- 3Congenital anomaly of face
- 3Congenital malformation
- 3Disorder of facial bone
- 3Disorder of head
- 3Disorder of musculoskeletal system
- 3Disorder of skeletal system
- 3Disorder of skull
- 3Finding of face
- 4Congenital anomaly of head
- 4Congenital anomaly of skeletal bone
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