Treatments & Interventions
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Colon cancer
Very frequent (80-99%)HP:0003003
Colorectal polyps
Very frequent (80-99%)HP:0200063
Congenital hypertrophy of retinal pigment epithelium
Very frequent (80-99%)HP:0007649
Gastrointestinal desmoid tumor
Very frequent (80-99%)HP:0100245
GI tract tumour
Very frequent (80-99%)HP:0007378
Multiple colonic adenomatous polyps
Very frequent (80-99%)HP:0005227
Dental problems
Frequent (30-79%)HP:0000164
Diarrhea
Frequent (30-79%)HP:0002014
Dyschezia
Frequent (30-79%)HP:0002019
Multiple duodenal polyps
Frequent (30-79%)HP:0004783
Multiple gastric polyps
Frequent (30-79%)HP:0004394
Osteoma
Frequent (30-79%)HP:0100246
Thyroid nodule
Frequent (30-79%)HP:0025388
Abnormality of the cementum
Occasional (5-29%)HP:0100717
Abnormality of the thyroid gland
Occasional (5-29%)HP:0000820
Adrenocortical adenoma
Occasional (5-29%)HP:0008256
Angiofibromas
Occasional (5-29%)HP:0010615
Breast fibroadenosis
Occasional (5-29%)HP:0010619
Duodenal adenocarcinoma
Occasional (5-29%)HP:0006771
Eruption failure
Occasional (5-29%)HP:0000706
Increased tooth count
Occasional (5-29%)HP:0011069
Neoplasm of the adrenal gland
Occasional (5-29%)HP:0100631
Papillary carcinoma of thyroid
Occasional (5-29%)HP:0002895
Rotting teeth
Occasional (5-29%)HP:0000670
Adenocarcinoma of the small intestine
Very rare (1-4%)HP:0040274
Biliary tract obstruction
Very rare (1-4%)HP:0005230
Brain tumor
Very rare (1-4%)HP:0030692
Cholangiocarcinoma
Very rare (1-4%)HP:0030153
Ependymoma
Very rare (1-4%)HP:0002888
Fatty lump
Very rare (1-4%)HP:0012032
Related Conditions
Gardner syndrome(child)
Turcot syndrome(child)
Attenuated familial adenomatous polyposis(child)
Serrated polyposis(child)
Familial adenomatous polyposis due to 5q22.2 microdeletion(child)
Digestive system hereditary disorder(parent)
Intestinal polyposis syndrome(parent)
Polyp of large intestine(parent)
Hereditary neoplastic syndrome(parent)
Quick Facts
- SNOMED CT
- 72900001
- UMLS CUI
- C0032580
- Fully Specified Name
- Familial multiple polyposis syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
- Known Treatments
- 1
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.