Deafness and oligodontia syndrome

disorder

SNOMED 715527006CUI C1857333

Overview

Deafness and oligodontia 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.

Partial anodontia

Very frequent (80-99%)HP:0000677

Sensorineural deafness

Very frequent (80-99%)HP:0000407

Dizziness

Frequent (30-79%)HP:0002321

Inner ear abnormality

Occasional (5-29%)HP:0000359

Bilateral congenital sensorineural deafness

HP:0008527

Gaps between teeth

HP:0000699

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Congenital sensorineural hearing loss(parent)

Developmental absence of tooth(parent)

Oligodontia(parent)

Hereditary hearing loss(parent)

Quick Facts

SNOMED CT: 715527006
UMLS CUI: C1857333
Fully Specified Name: Deafness and oligodontia syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 6

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.