OMOP Concept 36680611
Brachytelephalangic chondrodysplasia punctata
StandardConditionSNOMED778067002Disorder
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 Brachytelephalangic chondrodysplasia punctata via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C000705207 | Brachytelephalangic Chondrodysplasia Punctata | Non-standard |
Synonyms
Alternative names recorded for Brachytelephalangic chondrodysplasia punctata across source vocabularies.
- BCDP - brachytelephalangic chondrodysplasia punctata
- Brachytelephalangic chondrodysplasia punctata (disorder)
- condrodisplasia punteada braquitelefalángica
- condrodisplasia punteada braquitelefalángica (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(31)Roll up to these when you need a wider cohort.
- 1Chondrodysplasia punctata
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Inborn error of metabolism
- 1Metabolic bone disease
- 1X-linked recessive hereditary disease
- 2Congenital anomaly of skeletal bone
- 2Congenital disease
- 2Developmental disorder
- 2Disorder of bone
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hereditary metabolic disease
- 2Lesion of bone
- 2Metabolic disease
- 2Skeletal dysplasia
- 2X-linked hereditary disease
- 3Bone finding
- 3Congenital anomaly of musculoskeletal system
- 3Disease
- 3Disorder of body system
- 3Disorder of bone development
- 3Disorder of skeletal system
- 3Fetal and/or neonatal disorder
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