Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Robin sequence
Occasional (5-29%)
Acute neuronopathic Gaucher's disease
Frequent (30-79%)
Tracheobroncheopathia osteoplastica
Occasional (5-29%)
I-cell disease
Occasional (5-29%)
Marshall-Smith syndrome
Frequent (30-79%)
Camptomelic dysplasia
Frequent (30-79%)
Congenital junctional epidermolysis bullosa
Frequent (30-79%)
Opitz-Frias syndrome
Occasional (5-29%)
Pyknodysostosis
Occasional (5-29%)
Congenital absence of thyroid gland
Congenital tracheomalacia
Frequent (30-79%)
Scapuloperoneal spinal muscular atrophy
Multiple system atrophy
Frequent (30-79%)
Congenital myasthenia
Occasional (5-29%)
Congenital laryngeal abductor palsy
Congenital cleft larynx
Frequent (30-79%)
Generalized thyroid hormone resistance
D-2(OH) glutaric aciduria
Occasional (5-29%)
Anaplastic thyroid carcinoma
Occasional (5-29%)
Malignant lymphoma of thyroid gland
Frequent (30-79%)
Hypoplasia of thyroid
Hereditary nephritis
Very rare (1-4%)
Junctional epidermolysis bullosa gravis of Herlitz
Frequent (30-79%)
Recurrent respiratory papillomatosis
Occasional (5-29%)
Potassium aggravated myotonia
Quick Facts
- SNOMED CT
- 70407001
- UMLS CUI
- C0038450
- Fully Specified Name
- Stridor (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.