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.
Pigmentary pallidal degeneration
Frequent (30-79%)
Hereditary coproporphyria
Frequent (30-79%)
Diaphyseal dysplasia
Frequent (30-79%)
Metachromatic leukodystrophy, juvenile type
Occasional (5-29%)
Von Hippel-Lindau syndrome
Occasional (5-29%)
Spondyloepiphyseal dysplasia tarda
Occasional (5-29%)
Thromboangiitis obliterans
Complex regional pain syndrome
Very frequent (80-99%)
Encephalitis lethargica
Occasional (5-29%)
Presenile gangrene
Autosomal dominant sensory neuropathy
Frequent (30-79%)
Acute intermittent porphyria
Frequent (30-79%)
Spondylometaphyseal dysplasia - Sutcliffe type
Frequent (30-79%)
Metachromatic leukodystrophy
Occasional (5-29%)
Hereditary sensory and autonomic neuropathy type I
Frequent (30-79%)
Ehlers-Danlos syndrome classic type
Occasional (5-29%)
Dystonia 16
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
Adult-onset overlap myositis
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 90834002
- UMLS CUI
- C0030196
- Fully Specified Name
- Pain in limb (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.