Van der Woude syndrome

disorder

SNOMED 79261008CUI C0175697

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Lip pit

Very frequent (80-99%)HP:0100267

Cleft of palate

Frequent (30-79%)HP:0000175

Lower lip pit

Frequent (30-79%)HP:0000196

Cleft of upper lip

Occasional (5-29%)HP:0000204

Missing between one and six teeth

Occasional (5-29%)HP:0000668

Salivary gland disease

Occasional (5-29%)HP:0010286

Tongue tie

Occasional (5-29%)HP:0010296

Uvula bifida

Occasional (5-29%)HP:0000193

Related Conditions

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

Congenital anomaly of oral mucosa(parent)

Congenital anomaly of lip(parent)

Lesion of lip(parent)

Quick Facts

SNOMED CT: 79261008
UMLS CUI: C0175697
Fully Specified Name: Van der Woude syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 8

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.