OMOP Concept 37396269
Gollop syndrome
StandardConditionSNOMED716022002Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Gollop syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C538063 | Fronto-facio-nasal dysplasia | Non-standard |
| Nebraska Lexicon | 716022002 | Frontofacionasal dysplasia syndrome | Non-standard |
Synonyms
Alternative names recorded for Gollop syndrome across source vocabularies.
- Fronto-facio-nasal dysplasia
- Frontofacionasal dysplasia syndrome
- Frontofacionasal dysplasia syndrome (disorder)
- síndrome de displasia frontofacionasal
- síndrome de displasia frontofacionasal (trastorno)
- síndrome de Gollop
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(39)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Dysostosis of bone of skull
- 1Hereditary disorder of musculoskeletal system
- 1Multiple malformation syndrome with facial defects as major feature
- 2Autosomal hereditary disorder
- 2Congenital anomaly of face
- 2Congenital anomaly of skull
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Dysostosis
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple system malformation syndrome
- 3Congenital abnormality of skull and face bones
- 3Congenital anomaly of head
- 3Congenital anomaly of skeletal bone
- 3Congenital malformation syndrome
- 3Disease
- 3Disorder of body system
- 3Disorder of face
- 3Disorder of skull
- 3Genetic disease
- 3Musculoskeletal finding
- 3Skeletal dysplasia
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