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.
Arachnoid cyst
Occasional (5-29%)
Diaphyseal dysplasia
Always present (100%)
Pachyonychia congenita syndrome
Very frequent (80-99%)
Parkes Weber syndrome
Occasional (5-29%)
Idiopathic livedo reticularis with summer ulceration
Frequent (30-79%)
Spondyloenchondrodysplasia
Occasional (5-29%)
Spondyloenchondromatosis
Occasional (5-29%)
CARASIL syndrome
Frequent (30-79%)
Spastic paraplegia type 7
Very rare (1-4%)
Dysplasia of head of femur Meyer type
Occasional (5-29%)
Periodic fever and aphthous stomatitis with pharyngitis and cervical lymphadenitis syndrome
Occasional (5-29%)
Dystonia 16
Maternally inherited cardiomyopathy and deafness
Frequent (30-79%)
Autosomal recessive spastic paraplegia type 25
Frequent (30-79%)
Autosomal dominant hereditary spastic paraplegia
X-linked spastic paraplegia type 34
Frequent (30-79%)
Autosomal recessive spastic paraplegia type 62
Occasional (5-29%)
Charcot-Marie-Tooth disease, pyramidal features syndrome
Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia
Very frequent (80-99%)
NLR family pyrin domain containing 12-associated hereditary periodic fever syndrome
Frequent (30-79%)
Cataracts, motor neuropathy, short stature, skeletal anomalies syndrome
Occasional (5-29%)
Autosomal dominant Charcot-Marie-Tooth disease type 2V
Always present (100%)
Spinocerebellar ataxia type 43
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 10601006
- UMLS CUI
- C0023222
- Fully Specified Name
- Pain in lower limb (finding)
- Associated Conditions
- 23
- 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.