Overview
Congenital absence of nose 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.
Abnormally small eyeball
Frequent (30-79%)HP:0000568
Central cleft of nose
Frequent (30-79%)HP:0004122
Eyelid coloboma
Frequent (30-79%)HP:0000625
Failure of development of nasal septal cartilage
Frequent (30-79%)HP:0005273
Hypotrophic nasal bone
Frequent (30-79%)HP:0004646
Increased distance between eyes
Frequent (30-79%)HP:0000316
Laboured breathing
Frequent (30-79%)HP:0002098
Microtia
Frequent (30-79%)HP:0008551
Small nasal alae
Frequent (30-79%)HP:0000430
Tessier cleft
Frequent (30-79%)HP:0002006
Underdevelopment of nasal septum
Frequent (30-79%)HP:0009935
Missing nose
Occasional (5-29%)HP:0009927
Related Conditions
Quick Facts
- SNOMED CT
- 111317000
- UMLS CUI
- C0265740
- Fully Specified Name
- Congenital absence of nose (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 12
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.