OMOP Concept 4263588
Robin sequence
StandardConditionSNOMED4602007Disorder
Maps from
6
Descendants
6
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
6 source codes normalize to Robin sequence via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 127341 | Robin sequence | Non-standard |
| HPO | HP_0000201 | Pierre-Robin sequence | Non-standard |
| MeSH | D010855 | Pierre Robin Syndrome | Non-standard |
| OXMIS | 7560PR | SYNDROME PIERRE ROBIN | Non-standard |
| Read | PG0C.00 | Pierre - Robin syndrome | Non-standard |
| Read | PG0J.00 | Pierre Robin association | Non-standard |
Synonyms
Alternative names recorded for Robin sequence across source vocabularies.
- Micrognathia-glossoptosis syndrome
- Pierre Robin association
- Pierre Robin syndrome
- Robin sequence (disorder)
- síndrome de micrognatia - glosoptosis
- síndrome de Pierre Robin
- sucesión de Robin
- sucesión de Robin (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Multiple malformation syndrome with facial defects as major feature
- 2Congenital anomaly of face
- 2Multiple system malformation syndrome
- 3Congenital anomaly of head
- 3Congenital malformation syndrome
- 3Disorder of face
- 4Congenital malformation
- 4Disorder of head
- 4Finding of face
- 5Congenital disease
- 5Developmental disorder
- 5Disease
- 5Finding of head region
- 5Head finding
- 6Clinical finding
- 6Fetal and/or neonatal disorder
Narrower concepts
(6)Included automatically when you query with descendants.
- 1Intellectual disability, brachydactyly, Pierre Robin syndrome
- 1Joint contractures, developmental delay, Pierre Robin syndrome
- 1Pierre Robin sequence faciodigital anomaly syndrome
- 1Robin sequence and oligodactyly syndrome
- 1Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome
- 1Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome
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