OMOP Concept 4301299
Acrocephalopolysyndactyly type II
StandardConditionSNOMED403767009Disorder
Maps from
6
Descendants
0
Valid from
31 Jul 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
6 source codes normalize to Acrocephalopolysyndactyly type II via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C538142 | Summitt syndrome | Non-standard |
| MeSH | C563187 | Acrocephalopolysyndactyly Type II | Non-standard |
| Nebraska Lexicon | 403767009 | Acrocephalopolysyndactyly type 2 | Non-standard |
| Nebraska Lexicon | 733425005 | Acrocephalopolysyndactyly type IV | Non-standard |
| Nebraska Lexicon | 733606001 | Summitt's acrocephalosyndactyly | Non-standard |
| Read | PKy7000 | Carpenter's syndrome | Non-standard |
Synonyms
Alternative names recorded for Acrocephalopolysyndactyly type II across source vocabularies.
- acrocefalopolisindactilia tipo II
- acrocefalopolisindactilia tipo II (trastorno)
- Acrocephalopolysyndactyly type 2
- Acrocephalopolysyndactyly type II (disorder)
- Carpenter syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(43)Roll up to these when you need a wider cohort.
- 1Acrocephalopolysyndactyly
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 2Acrocephalosyndactyly
- 2Autosomal hereditary disorder
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Polysyndactyly
- 3Craniosynostosis syndrome
- 3Disease
- 3Disorder of body system
- 3Genetic disease
- 3Multiple malformation syndrome with limb defect as major feature
- 3Musculoskeletal finding
- 3Polydactyly
- 3Syndactyly
- 4Clinical finding
- 4Congenital anomaly of digit
- 4Imperfect fusion of skull
- 4Multiple system malformation syndrome
- 4Polymelia
- 5Congenital anomaly of head
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