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.
Subacute neuronopathic Gaucher's disease
Biotinidase deficiency
Occasional (5-29%)
Progressive sclerosing poliodystrophy
Frequent (30-79%)
Arginase deficiency
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Ectodermal dysplasia-ocular malformation syndrome
Frequent (30-79%)
Oculodentodigital syndrome
Frequent (30-79%)
Globoid cell leukodystrophy, late-onset
Frequent (30-79%)
Eales' disease
Occasional (5-29%)
Purine-nucleoside phosphorylase deficiency
Occasional (5-29%)
Cholestanol storage disease
Very rare (1-4%)
Mucopolysaccharidosis, MPS-I-H
Occasional (5-29%)
Mucopolysaccharidosis, MPS-I-S
Occasional (5-29%)
Mucopolysaccharidosis, MPS-I
Occasional (5-29%)
Amyotrophic lateral sclerosis
Occasional (5-29%)
Sjogren-Larsson syndrome
Always present (100%)
Galactosylceramide lipidosis
Frequent (30-79%)
Galactosylceramide beta-galactosidase deficiency
Frequent (30-79%)
Troyer syndrome
Frequent (30-79%)
Aicardi Goutieres syndrome
Occasional (5-29%)
Complex II deficiency
Occasional (5-29%)
Costeff syndrome
Frequent (30-79%)
Spinal arachnoiditis
Microphthalmia, cataract, radiculomegaly and septal heart defect
Occasional (5-29%)
Hypermanganesemia with dystonia, polycythaemia, and cirrhosis
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 312444006
- UMLS CUI
- C0037771
- Fully Specified Name
- Spastic paraparesis (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.