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.
African trypanosomiasis
Frequent (30-79%)
Cataplexy
Always present (100%)
Steinert myotonic dystrophy syndrome
Frequent (30-79%)
Trypanosomiasis
Frequent (30-79%)
Prader-Willi syndrome
Frequent (30-79%)
Multiple system atrophy
Frequent (30-79%)
Benson syndrome
Occasional (5-29%)
Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
Always present (100%)
Narcolepsy type 1
Frequent (30-79%)
SIM bHLH transcription factor 1-related Prader-Willi-like syndrome
Occasional (5-29%)
MAGE family member L2-related Prader-Willi-like syndrome
Occasional (5-29%)
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 69020003
- UMLS CUI
- C0392188
- Fully Specified Name
- Abnormal rapid eye movement sleep (finding)
- Associated Conditions
- 12
- 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.