OMOP Concept 36717401
Cardiocranial syndrome Pfeiffer type
StandardConditionSNOMED720606005Disorder
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 Cardiocranial syndrome Pfeiffer type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535578 | Cardiocranial syndrome | Non-standard |
| Nebraska Lexicon | 720606005 | Sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis | Non-standard |
Synonyms
Alternative names recorded for Cardiocranial syndrome Pfeiffer type across source vocabularies.
- Cardiocranial syndrome Pfeiffer type (disorder)
- Craniosynostosis with congenital heart disease and intellectual disability syndrome
- Pfeiffer Singer Zschiesche syndrome
- Sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis
- síndrome cardiocraneal tipo Pfeiffer
- síndrome cardiocraneal tipo Pfeiffer (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(52)Roll up to these when you need a wider cohort.
- 1Cardiovascular system hereditary disorder
- 1Congenital heart disease
- 1Craniosynostosis syndrome
- 1Developmental delay
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Multiple system malformation syndrome
- 2Congenital anomaly of cardiovascular structure of trunk
- 2Congenital anomaly of thorax
- 2Congenital malformation syndrome
- 2Developmental disorder
- 2Disorder of cardiovascular system
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Imperfect fusion of skull
- 2Structural disorder of heart
- 3Cardiovascular finding
- 3Congenital anomaly of cardiovascular system
- 3Congenital anomaly of head
- 3Congenital anomaly of joint
- 3Congenital anomaly of trunk
- 3Congenital anomaly of upper trunk
- 3Congenital malformation
- 3Cranial suture finding
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