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Familial adenomatous polyposis due to 5q22.2 microdeletion
ORPHA:261584
Classification level: Subtype of disorder- Synonym(s):
- Colorectal adenomatous polyposis due to monosomy 5q22.2
- FAP due to monosomy 5q22.2
- Familial adenomatous polyposis due to del(5)(q22.2)
- Familial adenomatous polyposis due to monosomy 5q22.2
- Familial polyposis coli due to monosomy 5q22.2
- Prevalence: -
- Inheritance: -
- Age of onset: -
- ICD-10: D12.6
- OMIM: -
- UMLS: -
- MeSH: -
- GARD: -
- MedDRA: -
Summary
This disease is described under Familial adenomatous polyposis
Detailed information
Article for general public
Professionals
- Clinical practice guidelines
- English (2012)
- Guidance for genetic testing
- English (2011)
- Clinical genetics review
- English (2017)
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.