Gingival fibromatosis with facial dysmorphism syndrome

disorder

SNOMED 719687007CUI C4304501

Overview

Gingival fibromatosis with facial dysmorphism 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.

Big calvaria

Very frequent (80-99%)HP:0000256

Delayed eruption of teeth

Very frequent (80-99%)HP:0000684

Depressed nasal root/bridge

Very frequent (80-99%)HP:0005280

Down-slanting palpebral fissure

Very frequent (80-99%)HP:0000494

Gingival fibromatosis

Very frequent (80-99%)HP:0000169

Gingival overgrowth

Very frequent (80-99%)HP:0000212

High arched palate

Very frequent (80-99%)HP:0000218

Increased distance between eyes

Very frequent (80-99%)HP:0000316

Misshapened teeth

Very frequent (80-99%)HP:0006482

Small nasal alae

Very frequent (80-99%)HP:0000430

Thick eyebrow

Very frequent (80-99%)HP:0000574

Unibrow

Very frequent (80-99%)HP:0000664

Cupid-bow shaped upper lip

Frequent (30-79%)HP:0002263

Eclabium of lower lip

Frequent (30-79%)HP:0000232

Related Conditions

Multiple malformation syndrome with facial defects as major feature(parent)

Recessive hereditary disorder (autosomal)(parent)

Hereditary gingival fibromatosis(parent)

Developmental hereditary disorder(parent)

Disorder of digestive system specific to fetus OR newborn(parent)

Quick Facts

SNOMED CT: 719687007
UMLS CUI: C4304501
Fully Specified Name: Gingival fibromatosis with facial dysmorphism syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 14

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.