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.
Arginase deficiency
Always present (100%)
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Occasional (5-29%)
Fucosidosis
Always present (100%)
Adrenoleukodystrophy
Frequent (30-79%)
Isaacs syndrome
Primary lateral sclerosis
Frequent (30-79%)
Silver disease
Frequent (30-79%)
Troyer syndrome
Occasional (5-29%)
Neuromyotonia
Episodic ataxia type 1
PPMX - Mental retardation with psychosis, pyramidal signs, and macroorchidism
ARSACS - autosomal recessive spastic ataxia of Charlevoix-Saguenay
Always present (100%)
Spastic paraplegia type 7
Very frequent (80-99%)
Juvenile primary lateral sclerosis
Very frequent (80-99%)
X-linked spastic paraplegia type 2
Very frequent (80-99%)
Autosomal dominant spastic paraplegia type 36
Very frequent (80-99%)
Autosomal dominant spastic paraplegia type 4
Autosomal recessive spastic paraplegia type 44
Always present (100%)
Autosomal recessive spastic paraplegia type 46
Autosomal recessive spastic paraplegia type 54
Frequent (30-79%)
Intellectual disability Buenos Aires type
Very frequent (80-99%)
Autosomal recessive spastic paraplegia type 32
Autosomal recessive spastic paraplegia type 26
Autosomal recessive spastic paraplegia type 23
Frequent (30-79%)
Spastic paraplegia with Paget disease of bone syndrome
Always present (100%)
Quick Facts
- SNOMED CT
- 9447003
- UMLS CUI
- C0231687
- Fully Specified Name
- Spastic gait (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.