Overview
Apnea is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Mohr syndrome
Occasional (5-29%)
Stiff-man syndrome
Occasional (5-29%)
Biotinidase deficiency
Occasional (5-29%)
Acute neuronopathic Gaucher's disease
Frequent (30-79%)
Methylcrotonyl-CoA carboxylase deficiency
Fructose-biphosphatase deficiency
Schwartz-Jampel syndrome
Occasional (5-29%)
Ehlers-Danlos syndrome, type 3
Occasional (5-29%)
Infantile hypophosphatasia
Rett's disorder
Propionic acidemia
Marshall-Smith syndrome
Camptomelic dysplasia
Frequent (30-79%)
Mucopolysaccharidosis, MPS-I
Frequent (30-79%)
Fatal familial insomnia
Congenital absence of adrenal gland
Congenital tracheomalacia
Very rare (1-4%)
Deficiency of tryptophan decarboxylase
Frequent (30-79%)
Deficiency of propionyl-CoA carboxylase
Benign neonatal familial convulsions
Frequent (30-79%)
Alternating hemiplegia of childhood
Occasional (5-29%)
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
Always present (100%)
Familial aplasia of the vermis
Very frequent (80-99%)
LVA - Congenital left ventricular aneurysm
Occasional (5-29%)
Stuve-Wiedemann dysplasia
Frequent (30-79%)
Related Symptoms
Quick Facts
- SNOMED CT
- 1023001
- UMLS CUI
- C0003578
- Fully Specified Name
- Apnea (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.