OMOP Concept 604944
Pfeiffer syndrome type 2
StandardConditionSNOMED1003916008Disorder
Maps from
0
Descendants
0
Valid from
31 Jan 2021
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Pfeiffer syndrome type 2 across source vocabularies.
- Pfeiffer syndrome type 2 (disorder)
- síndrome de Pfeiffer tipo 2
- síndrome de Pfeiffer tipo 2 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(40)Roll up to these when you need a wider cohort.
- 1Acrocephalosyndactyly type V
- 2Acrocephalosyndactyly
- 2Autosomal dominant hereditary disorder
- 2Developmental hereditary disorder
- 2Hereditary disorder of musculoskeletal system
- 3Autosomal hereditary disorder
- 3Craniosynostosis syndrome
- 3Developmental disorder
- 3Disorder of musculoskeletal system
- 3Genetic disease
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Multiple malformation syndrome with limb defect as major feature
- 3Syndactyly
- 4Congenital anomaly of digit
- 4Disease
- 4Disorder of body system
- 4Imperfect fusion of skull
- 4Multiple system malformation syndrome
- 4Musculoskeletal finding
- 5Clinical finding
- 5Congenital anomaly of head
- 5Congenital anomaly of joint
- 5Congenital anomaly of limb
- 5Congenital malformation syndrome
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