Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Astrocytoma
Very frequent (80-99%)HP:0009592
Multiple flat light-brown marks on skin
Very frequent (80-99%)HP:0007565
Absence of corpus callosum
Frequent (30-79%)HP:0001274
Glioblastoma
Frequent (30-79%)HP:0012174
Gray matter heterotopias
Frequent (30-79%)HP:0002282
Multiple colonic adenomatous polyps
Frequent (30-79%)HP:0005227
Non-Hodgkin lymphoma
Frequent (30-79%)HP:0012539
T-cell lymphoma
Frequent (30-79%)HP:0012190
Adenocarcinoma of the colon
Occasional (5-29%)HP:0040276
Adenocarcinoma of the small intestine
Occasional (5-29%)HP:0040274
Axillary freckling
Occasional (5-29%)HP:0000997
Blood cancer
Occasional (5-29%)HP:0001909
Cancer of lymphatic system
Occasional (5-29%)HP:0002665
Hypopigmentation of the skin
Occasional (5-29%)HP:0001010
Oligodendroglioma
Occasional (5-29%)HP:0033681
Pleomorphic xanthoastrocytoma
Occasional (5-29%)HP:0033682
Plexiform neurofibroma
Occasional (5-29%)HP:0009732
Basal cell nevus
HP:0002671
Cancer of early nerve cells
HP:0003006
Ependymoma
HP:0002888
Medulloblastoma
HP:0002885
Rhabdomyosarcoma
HP:0002859
Quick Facts
- SNOMED CT
- 61665008
- UMLS CUI
- C0265325
- Fully Specified Name
- Turcot syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 22
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.