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.
Brachial plexus lesion
Very frequent (80-99%)
Neuralgic amyotrophy
Very frequent (80-99%)
Globoid cell leukodystrophy, late-onset
Occasional (5-29%)
Von Hippel-Lindau syndrome
Occasional (5-29%)
Acute transverse myelitis
Occasional (5-29%)
Amyotrophic lateral sclerosis
Frequent (30-79%)
Nemaline myopathy, late onset type
Frequent (30-79%)
Encephalitis lethargica
Frequent (30-79%)
Troyer syndrome
Frequent (30-79%)
Aneurysm of carotid artery
Occasional (5-29%)
Acute poliomyelitis
Occasional (5-29%)
Neurogenic arthrogryposis multiplex congenita
Frequent (30-79%)
Hereditary motor and sensory neuropathy Okinawa type
Very frequent (80-99%)
Spastic paraplegia type 7
Occasional (5-29%)
Charcot-Marie-Tooth disease type 4C
Charcot-Marie-Tooth disease type 4H
Autosomal dominant Charcot-Marie-Tooth disease type 2D
Autosomal dominant Charcot-Marie-Tooth disease type 2E
Very frequent (80-99%)
Autosomal dominant Charcot-Marie-Tooth disease type 2I
Choroideremia with deafness and obesity syndrome
Occasional (5-29%)
Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
Frequent (30-79%)
Charcot-Marie-Tooth disease type ID
Autosomal recessive spastic paraplegia type 55
Frequent (30-79%)
Charcot-Marie-Tooth disease type 2B1
Autosomal recessive spastic paraplegia type 26
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 713512009
- UMLS CUI
- C1698196
- Fully Specified Name
- Muscle weakness of upper limb (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.