OMOP Concept 36715115
Camptodactyly syndrome Guadalajara type 1
StandardConditionSNOMED720602007Disorder
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 Camptodactyly syndrome Guadalajara type 1 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537970 | Camptodactyly syndrome Guadalajara type 1 | Non-standard |
Synonyms
Alternative names recorded for Camptodactyly syndrome Guadalajara type 1 across source vocabularies.
- Camptodactyly syndrome Guadalajara type 1 (disorder)
- síndrome de camptodactilia tipo Guadalajara 1
- síndrome de camptodactilia tipo Guadalajara 1 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(57)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Camptodactyly
- 1Congenital anomaly of finger
- 1Congenital deformity of hand
- 1Developmental hereditary disorder
- 1Finding of musculoskeletal structure of digit of hand
- 1Flexion deformity of hand
- 1Hereditary disorder of musculoskeletal system
- 1Multiple malformation syndrome with facial-limb defects as major feature
- 2Autosomal hereditary disorder
- 2Congenital abnormal shape of digit
- 2Congenital anomaly of digit
- 2Congenital anomaly of hand
- 2Congenital anomaly of limb
- 2Congenital deformity of musculoskeletal system
- 2Congenital deformity of upper limb
- 2Deformity of hand
- 2Deformity of limb
- 2Developmental disorder
- 2Disorder of finger
- 2Disorder of musculoskeletal system
- 2Finding of digit of hand
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple malformation syndrome with facial defects as major feature
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