OMOP Concept 37204832
Heart defect, tongue hamartoma, polysyndactyly syndrome
StandardConditionSNOMED783738002Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2019
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Heart defect, tongue hamartoma, polysyndactyly syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535849 | Heart defect, tongue hamartoma and polysyndactyly | Non-standard |
Synonyms
Alternative names recorded for Heart defect, tongue hamartoma, polysyndactyly syndrome across source vocabularies.
- Heart defect, tongue hamartoma, polysyndactyly syndrome (disorder)
- Ostravik Lindemann Solberg syndrome
- síndrome de defecto cardíaco, hamartoma de lengua y polisindactilia
- síndrome de defecto cardíaco, hamartoma de lengua y polisindactilia (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(73)Roll up to these when you need a wider cohort.
- 1Congenital heart disease
- 1Disorder of digestive system specific to fetus OR newborn
- 1Genetic disease
- 1Hamartoma of tongue
- 1Multiple malformation syndrome with limb defect as major feature
- 1Polysyndactyly
- 2Congenital anomaly of cardiovascular structure of trunk
- 2Congenital anomaly of thorax
- 2Disease
- 2Disorder of digestive system
- 2Fetal and/or neonatal disorder
- 2Hamartoma
- 2Lesion of tongue
- 2Mass of tongue
- 2Multiple system malformation syndrome
- 2Polydactyly
- 2Structural disorder of heart
- 2Syndactyly
- 3Clinical finding
- 3Congenital anomaly of cardiovascular system
- 3Congenital anomaly of digit
- 3Congenital anomaly of trunk
- 3Congenital anomaly of upper trunk
- 3Congenital malformation syndrome
- 3Digestive system finding
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