OMOP Concept 37110773
Atelosteogenesis type 1
StandardConditionSNOMED725141006Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Atelosteogenesis type 1 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535396 | Atelosteogenesis, type 1 | Non-standard |
| Nebraska Lexicon | 725141006 | Giant cell chondrodysplasia | Non-standard |
Synonyms
Alternative names recorded for Atelosteogenesis type 1 across source vocabularies.
- atelosteogénesis tipo 1
- atelosteogénesis tipo 1 (trastorno)
- Atelosteogenesis type 1 (disorder)
- Atelosteogenesis type I
- Giant cell chondrodysplasia
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(41)Roll up to these when you need a wider cohort.
- 1Atelosteogenesis
- 1Bone injury
- 1Congenital anomaly of skeletal bone
- 2Congenital anomaly of musculoskeletal system
- 2Developmental hereditary disorder
- 2Disorder of bone
- 2Disorder of bone development
- 2Hereditary disorder of musculoskeletal system
- 2Injury of musculoskeletal system
- 2Multiple dislocations with dysplasia
- 2Osteochondrodysplasia syndrome
- 3Bone finding
- 3Chronic arthropathy
- 3Congenital malformation
- 3Developmental disorder
- 3Disorder of musculoskeletal system
- 3Disorder of skeletal system
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Multiple system malformation syndrome
- 3Pathological dislocation of multiple joints
- 3Skeletal dysplasia
- 3Traumatic or non-traumatic injury
- 4Arthropathy
- 4Chronic disease of musculoskeletal system
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