OMOP Concept 4035173
Coffin-Lowry syndrome
StandardConditionSNOMED15182000Disorder
Maps from
4
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
4 source codes normalize to Coffin-Lowry syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 144632 | Coffin-Lowry syndrome | Non-standard |
| MeSH | D038921 | Coffin-Lowry Syndrome | Non-standard |
| Nebraska Lexicon | 15182000 | CLS - Coffin-Lowry syndrome | Non-standard |
| Read | PKy5F00 | Coffin-Lowry syndrome | Non-standard |
Synonyms
Alternative names recorded for Coffin-Lowry syndrome across source vocabularies.
- CLS - Coffin-Lowry syndrome
- Coffin-Lowry syndrome (disorder)
- síndrome de Coffin - Lowry
- síndrome de Coffin - Lowry (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(50)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of hand
- 1Congenital anomaly of musculoskeletal system
- 1Disorder of skeletal system
- 1Genetic disease
- 1Global developmental delay
- 1Intellectual disability
- 1Multiple malformation syndrome with facial-limb defects as major feature
- 1Short stature disorder
- 2Behavior finding
- 2Congenital anomaly of limb
- 2Congenital anomaly of upper limb
- 2Congenital malformation
- 2Developmental delay
- 2Disease
- 2Disorder of hand
- 2Disorder of musculoskeletal system
- 2Disorder of stature
- 2Impaired cognition
- 2Intellectual ability - finding
- 2Multiple malformation syndrome with facial defects as major feature
- 2Multiple malformation syndrome with limb defect as major feature
- 2Neurodevelopmental disorder
- 3Clinical finding
- 3Cognitive function finding
- 3Congenital anomaly of face
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