Congenital laryngeal abductor palsy

disorder

SNOMED 232442001CUI C0396059

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Laryngomalacia

Very frequent (80-99%)HP:0001601

Respiratory insufficiency

Frequent (30-79%)HP:0002093

Foot, talipes equinovarus

Very rare (1-4%)HP:0001762

Blue discoloration of the skin

HP:0000961

Decreased size of cranium

HP:0000252

Deglutition disorder

HP:0002015

Dull intelligence

HP:0001249

Husky voice

HP:0001609

Laryngeal paralysis

HP:0001605

Noisy breathing

HP:0010307

Quiet voice

HP:0001621

Related Conditions

Laryngeal abductor paralysis with intellectual disability syndrome(child)

Congenital disease(parent)

Disease of skeletal muscle(parent)

Musculoskeletal disorder of the neck(parent)

Disorder of larynx(parent)

Movement disorder(parent)

Perinatal respiratory disorders(parent)

Quick Facts

SNOMED CT: 232442001
UMLS CUI: C0396059
Fully Specified Name: Congenital laryngeal abductor palsy (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.