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Beckwith-Wiedemann syndrome due to imprinting defect of 11p15
ORPHA:231117
Classification level: Subtype of disorder- Synonym(s): -
- Prevalence: -
- Inheritance: -
- Age of onset: Infancy, Neonatal
- ICD-10: Q87.3
- OMIM: -
- UMLS: -
- MeSH: -
- GARD: -
- MedDRA: -
Summary
This disease is described under Beckwith-Wiedemann syndrome
Detailed information
Article for general public
Professionals
- Anesthesia guidelines
- Czech (2013)
- English (2013)
- Español (2013)
- Review article
- Español (2015, pdf)
- Clinical practice guidelines
- English (2018)
- Guidance for genetic testing
- English (2013)
- Clinical genetics review
- English (2016)
Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
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