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.
Troyer syndrome
Juvenile amyotrophic lateral sclerosis
Very frequent (80-99%)
Congenital pontocerebellar hypoplasia type 6
Autosomal recessive spastic paraplegia type 44
Always present (100%)
Autosomal recessive spastic paraplegia type 46
Occasional (5-29%)
Autosomal recessive spastic paraplegia type 54
Frequent (30-79%)
Autosomal recessive spastic paraplegia type 26
Frequent (30-79%)
Autosomal recessive spastic paraplegia type 18
Autosomal dominant spastic paraplegia type 10
Very rare (1-4%)
Autosomal dominant spastic paraplegia type 29
Autosomal dominant spastic paraplegia type 37
Occasional (5-29%)
Autosomal recessive spastic paraplegia type 5A
Very rare (1-4%)
Spastic paraplegia, retinal degeneration syndrome
Frequent (30-79%)
Autosomal dominant spastic paraplegia type 8
Occasional (5-29%)
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome
Very frequent (80-99%)
Autosomal recessive spastic paraplegia type 76
Frequent (30-79%)
Raynaud Claes syndrome
Very rare (1-4%)
Posterior meningocele
Occasional (5-29%)
Juvenile amyotrophic lateral sclerosis type 2
X-linked intellectual disability, short stature, overweight syndrome
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 394680009
- UMLS CUI
- C1273957
- Fully Specified Name
- Upper limb spasticity (finding)
- Associated Conditions
- 20
- 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.