OMOP Concept 36715273
Craniosynostosis Philadelphia type
StandardConditionSNOMED720818003Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Craniosynostosis Philadelphia type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563368 | Craniosynostosis, Philadelphia Type | Non-standard |
| Nebraska Lexicon | 720818003 | Craniosynostosis Philadelphia type | Non-standard |
Synonyms
Alternative names recorded for Craniosynostosis Philadelphia type across source vocabularies.
- craneosinostosis tipo Filadelfia
- craneosinostosis tipo Filadelfia (trastorno)
- Craniosynostosis Philadelphia type (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(48)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital abnormality of skull shape
- 1Congenital anomaly of bone and joint
- 1Craniosynostosis syndrome
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Multiple malformation syndrome with limb defect as major feature
- 1Syndactyly
- 2Autosomal hereditary disorder
- 2Congenital anomaly of digit
- 2Congenital anomaly of joint
- 2Congenital anomaly of skeletal bone
- 2Congenital anomaly of skull
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Imperfect fusion of skull
- 2Multiple system malformation syndrome
- 3Arthropathy
- 3Congenital abnormality of skull and face bones
- 3Congenital anomaly of head
- 3Congenital anomaly of limb
- 3Congenital anomaly of musculoskeletal system
- 3Congenital malformation syndrome
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