Overview
Hereditary gingival fibromatosis is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Gingival fibromatosis
Very frequent (80-99%)HP:0000169
Gingival hyperplasia
Very frequent (80-99%)HP:0000212
Deafness
Excluded (<1%)HP:0000365
Dull intelligence
Excluded (<1%)HP:0001249
Related Conditions
Gingival fibromatosis and hypertrichosis syndrome(child)
Gingival fibromatosis with facial dysmorphism syndrome(child)
Gingival fibromatosis with progressive deafness syndrome(child)
Digestive system hereditary disorder(parent)
Autosomal hereditary disorder(parent)
Gingival fibromatosis(parent)
Non-plaque induced gingival disease(parent)
Quick Facts
- SNOMED CT
- 109620006
- UMLS CUI
- C0399440
- Fully Specified Name
- Hereditary gingival fibromatosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 4
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.