Gingival fibromatosis and hypertrichosis syndrome

disorder

SNOMED 716008002CUI C4274889

Overview

Gingival fibromatosis and hypertrichosis syndrome 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.

Generalized hirsutism

Very frequent (80-99%)HP:0002230

Hirsutism

Very frequent (80-99%)HP:0001007

Idiopathic gingival hyperplasia

Very frequent (80-99%)HP:0000169

Coarse face

Frequent (30-79%)HP:0000280

Delayed eruption of teeth

Frequent (30-79%)HP:0000684

Electroencephalogram abnormal

Frequent (30-79%)HP:0002353

Oral soft tissue hyperplasia

Frequent (30-79%)HP:0000212

Tooth abnormalities

Frequent (30-79%)HP:0000164

Ataxia

Occasional (5-29%)HP:0001251

Cognitive deficits

Occasional (5-29%)HP:0100543

Epilepsy

Occasional (5-29%)HP:0001250

Thick eyebrow

Occasional (5-29%)HP:0000574

Unibrow

Occasional (5-29%)HP:0000664

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hypertrichosis(parent)

Hereditary gingival fibromatosis(parent)

Hereditary disorder of the integument(parent)

Quick Facts

SNOMED CT: 716008002
UMLS CUI: C4274889
Fully Specified Name: Gingival fibromatosis and hypertrichosis syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

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.