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Non-hereditary retinoblastoma
ORPHA:357034
Classification level: Subtype of disorder- Synonym(s): -
- Prevalence: Unknown
- Inheritance: Not applicable
- Age of onset: Infancy, Neonatal
- ICD-10: C69.2
- OMIM: 180200
- UMLS: -
- MeSH: -
- GARD: -
- MedDRA: -
Summary
This disease is described under Retinoblastoma
Detailed information
Article for general public
Professionals
- Review article
- English (2006)
- Clinical practice guidelines
- English (2009, pdf)
- Français (2009, pdf)
- Guidance for genetic testing
- English (2010)
- Clinical genetics review
- English (2018)
- Disability factsheet
- Français (2016, 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.