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Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
ORPHA:98754
Classification level: Subtype of disorder- Synonym(s):
- UPD(15)mat
- Prevalence: -
- Inheritance: -
- Age of onset: Adolescent, Adult
- ICD-10: Q87.1
- OMIM: 176270
- UMLS: -
- MeSH: -
- GARD: -
- MedDRA: -
Summary
This disease is described under Prader-Willi syndrome
Detailed information
Article for general public
Professionals
- Emergency guidelines
- Français (2012, pdf)
- Anesthesia guidelines
- Deutsch (2012)
- Czech (2012)
- English (2021)
- Español (2021)
- Review article
- Español (2015, pdf)
- Clinical practice guidelines
- Français (2021)
- English (2017)
- Deutsch (2010)
- Practical genetics
- English (2008, pdf)
- Guidance for genetic testing
- English (2014)
- Clinical genetics review
- English (2017)
- Disability factsheet
- Español (2017, pdf)
- Français (2013, pdf)
Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.