OMOP Concept 36715268
Craniosynostosis, anal anomaly, porokeratosis syndrome
StandardConditionSNOMED720812002Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Craniosynostosis, anal anomaly, porokeratosis syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536789 | Craniosynostosis, anal anomalies, and porokeratosis | Non-standard |
Synonyms
Alternative names recorded for Craniosynostosis, anal anomaly, porokeratosis syndrome across source vocabularies.
- CDAGS (craniosynostosis, clavicular hypoplasia, delayed closure of fontanelle, anal anomalies, genitourinary malformations, skin eruption) syndrome
- CDAGS syndrome
- Craniosynostosis, anal anomaly, porokeratosis syndrome (disorder)
- síndrome de craneosinostosis, anomalía anal y poroqueratosis
- síndrome de craneosinostosis, anomalía anal y poroqueratosis (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(36)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Craniosynostosis syndrome
- 1Developmental hereditary disorder
- 1Disorder of skull
- 1Hereditary disorder of musculoskeletal system
- 1Multiple system malformation syndrome
- 2Autosomal hereditary disorder
- 2Congenital malformation syndrome
- 2Developmental disorder
- 2Disorder of bone
- 2Disorder of head
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Imperfect fusion of skull
- 2Skull finding
- 3Bone finding
- 3Congenital anomaly of head
- 3Congenital anomaly of joint
- 3Congenital malformation
- 3Cranial suture finding
- 3Disease
- 3Disorder of body system
- 3Disorder of skeletal system
- 3Genetic disease
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