Overview
Microtia 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.
Microtia
Always present (100%)HP:0008551
Unilateral conductive hearing impairment
Very frequent (80-99%)HP:0040119
Anotia
Frequent (30-79%)HP:0009892
Delayed language development
Frequent (30-79%)HP:0000750
Dysplastic ears
Frequent (30-79%)HP:0000377
External auditory meatal atresia
Frequent (30-79%)HP:0000413
Hypoplastic helices
Frequent (30-79%)HP:0008589
Childhood attention deficit/hyperactivity disorder
Occasional (5-29%)HP:0007018
Single brain ventricle
Occasional (5-29%)HP:0001360
Related Conditions
Bilateral microtia with deafness and cleft palate syndrome(child)
Hypertelorism with microtia and facial clefting syndrome(child)
Isotretinoin-like syndrome(child)
Thickened earlobe with conductive deafness syndrome(child)
Microtia, eye coloboma, imperforation of nasolacrimal duct syndrome(child)
Coxoauricular syndrome(child)
Congenital deafness with inner ear agenesis, microtia, and microdontia(child)
Microphthalmia, microtia, foetal akinesia syndrome(child)
Congenital abnormality of external ear(parent)
Quick Facts
- SNOMED CT
- 35045004
- UMLS CUI
- C0152423
- Fully Specified Name
- Microtia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 9
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.