Oculootodental syndrome

disorder

SNOMED 770944002CUI C2750325

Overview

Oculootodental 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.

Notched pupil

Occasional (5-29%)HP:0000589

Absence of bicuspid

HP:0011051

Delayed eruption of teeth

HP:0000684

Increased length of philtrum

HP:0000343

Large elongated pulp chamber

HP:0000679

Nostrils anteverted

HP:0000463

Pulpoliths

HP:0003771

Sensorineural deafness

HP:0000407

Thin dental enamel

HP:0006297

Tooth ankylosis

HP:0033791

Vertical enlargement of face

HP:0000276

Related Conditions

Globodontia(parent)

Congenital sensorineural hearing loss(parent)

Hearing loss associated with syndrome(parent)

Deletion of part of chromosome 11(parent)

Disorder of ear(parent)

Congenital malformation(parent)

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

Quick Facts

SNOMED CT: 770944002
UMLS CUI: C2750325
Fully Specified Name: Oculootodental syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 11

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.