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.
Progressive sclerosing poliodystrophy
Frequent (30-79%)
Polycystic kidney disease, infantile type
Occasional (5-29%)
Post poliomyelitis syndrome
Very rare (1-4%)
Duchenne muscular dystrophy
Prader-Willi syndrome
Merosin deficient congenital muscular dystrophy
Occasional (5-29%)
Extreme obesity with alveolar hypoventilation
Becker muscular dystrophy
CCHS - Congenital central hypoventilation
Always present (100%)
Perry syndrome
Frequent (30-79%)
Charcot-Marie-Tooth disease type 4C
Occasional (5-29%)
Bethlem myopathy
Occasional (5-29%)
Haddad syndrome
Always present (100%)
Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation
Occasional (5-29%)
Purine rich element binding protein A syndrome
Frequent (30-79%)
Severe neonatal hypotonia, seizures, encephalopathy syndrome due to 5q31.3 microdeletion
Occasional (5-29%)
ROHHADNET (rapid-onset childhood obesity, hypothalamic dysfunction, hypoventilation, autonomic dysregulation, neural tumours) syndrome
Very frequent (80-99%)
Merosin-negative congenital muscular dystrophy
Occasional (5-29%)
Proximal spinal muscular atrophy
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 80954004
- UMLS CUI
- C0235063
- Fully Specified Name
- Decreased respiratory function (finding)
- Associated Conditions
- 19
- 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.