OMOP Concept 37396051
Brachydactyly type A1
StandardConditionSNOMED715720006Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Brachydactyly type A1 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| HPO | HP_0009371 | Type A1 brachydactyly | Non-standard |
| MeSH | C537088 | Brachydactyly type A1 | Non-standard |
Synonyms
Alternative names recorded for Brachydactyly type A1 across source vocabularies.
- Brachydactyly Farabee type
- Brachydactyly type A1 (disorder)
- braquidactilia tipo A1
- braquidactilia tipo A1 (trastorno)
- braquidactilia tipo Farabee
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.
- 1Autosomal dominant hereditary disorder
- 1Brachyphalangia
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 2Abnormally short long bone
- 2Autosomal hereditary disorder
- 2Brachydactyly
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Structural abnormality of bone of limb
- 3Abnormally short digit
- 3Congenital anomaly of skeletal bone
- 3Congenital deformity of musculoskeletal system
- 3Deformation of bone
- 3Disease
- 3Disorder of body system
- 3Disorder of bone
- 3Disorder of limb
- 3Genetic disease
- 3Musculoskeletal finding
- 3Structural abnormality of long bone
- 3Structural abnormality of skeleton
- 4Bone finding
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