OMOP Concept 4271182
Frontometaphyseal dysplasia
StandardConditionSNOMED62803002Disorder
Maps from
5
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
5 source codes normalize to Frontometaphyseal dysplasia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 139792 | Frontometaphyseal dysplasia | Non-standard |
| MeSH | C538064 | Frontometaphyseal dysplasia | Non-standard |
| Nebraska Lexicon | 62803002 | Frontometaphyseal dysplasia | Non-standard |
| Read | PG45.14 | Frontometaphyseal dysostosis | Non-standard |
| Read | PG5E.00 | Frontometaphyseal dysplasia | Non-standard |
Synonyms
Alternative names recorded for Frontometaphyseal dysplasia across source vocabularies.
- displasia frontometafisaria
- displasia frontometafisaria (trastorno)
- FMD - Frontometaphyseal dysplasia
- Frontometaphyseal dysplasia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(38)Roll up to these when you need a wider cohort.
- 1Dysplasia with increased bone density
- 1Osteochondrodysplasia syndrome
- 1Otopalatodigital syndrome spectrum disorder
- 2Bone density above reference range
- 2Congenital anomaly of skeletal bone
- 2Developmental hereditary disorder
- 2Disorder of bone
- 2Hereditary disorder of musculoskeletal system
- 2Multiple system malformation syndrome
- 2Skeletal dysplasia
- 2X-linked dominant hereditary disease
- 3Bone densimetry abnormal
- 3Bone density finding
- 3Bone finding
- 3Congenital anomaly of musculoskeletal system
- 3Congenital malformation syndrome
- 3Developmental disorder
- 3Disorder of bone development
- 3Disorder of musculoskeletal system
- 3Disorder of skeletal system
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Measurement finding above reference range
- 3X-linked hereditary disease
- 4Congenital malformation
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