Congenital cleft larynx

disorder

SNOMED 232461002CUI C1840311

Overview

Congenital cleft larynx 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.

Laryngotracheal cleft

Always present (100%)HP:0008751

Blue discoloration of the skin

Frequent (30-79%)HP:0000961

Choking episodes

Frequent (30-79%)HP:0030842

Coughing

Frequent (30-79%)HP:0012735

Hoarse cry

Frequent (30-79%)HP:0001615

Impaired oropharyngeal swallow response

Frequent (30-79%)HP:0031162

Laryngomalacia

Frequent (30-79%)HP:0001601

Noisy breathing

Frequent (30-79%)HP:0010307

Panting

Frequent (30-79%)HP:0002094

Pulmonary aspiration

Frequent (30-79%)HP:0002835

respiratory infections, recurrent

Frequent (30-79%)HP:0002205

Voice abnormality

Frequent (30-79%)HP:0001608

Respiratory distress, neonatal

Occasional (5-29%)HP:0002643

Related Conditions

Opitz-Frias syndrome(child)

Congenital cleft of posterior cricoid cartilage(child)

Congenital laryngocele(child)

Congenital cleft thyroid cartilage(child)

Congenital anomaly of larynx(parent)

Lesion of larynx(parent)

Quick Facts

SNOMED CT: 232461002
UMLS CUI: C1840311
Fully Specified Name: Congenital cleft larynx (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

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.