Overview
Spinocerebellar ataxia type 13 is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Appendicular ataxia
Frequent (30-79%)HP:0002070
Decreased distal vibration sense
Frequent (30-79%)HP:0006886
Degeneration of cerebellum
Frequent (30-79%)HP:0001272
Delayed motor milestones
Frequent (30-79%)HP:0001270
Difficulty articulating speech
Frequent (30-79%)HP:0001260
Difficulty running
Frequent (30-79%)HP:0009046
Gait disturbance
Frequent (30-79%)HP:0001288
Generalised decreased muscle tone
Frequent (30-79%)HP:0001290
Impaired visuospatial constructive cognition
Frequent (30-79%)HP:0010794
Inability to coordinate movements when walking
Frequent (30-79%)HP:0002066
Increased reflexes
Frequent (30-79%)HP:0001347
Intellectual impairment
Frequent (30-79%)HP:0100543
Involuntary, rapid, rhythmic eye movements
Frequent (30-79%)HP:0000639
Mental retardation, mild
Frequent (30-79%)HP:0001256
Psychomotor development deficiency
Frequent (30-79%)HP:0001263
Titubation
Frequent (30-79%)HP:0030187
Clumsiness
Occasional (5-29%)HP:0002312
Deglutition disorder
Occasional (5-29%)HP:0002015
Hearing impairment
Occasional (5-29%)HP:0000365
Hyperactive deep tendon reflexes
Occasional (5-29%)HP:0006801
Involuntary muscle stiffness, contraction, or spasm
Occasional (5-29%)HP:0001257
Jerking
Occasional (5-29%)HP:0001336
Optic disc pallor
Occasional (5-29%)HP:0000543
Postural instability
Occasional (5-29%)HP:0002172
Spasmodic torticollis
Occasional (5-29%)HP:0000473
Urinary incontinence
Occasional (5-29%)HP:0000020
Urinary urgency
Occasional (5-29%)HP:0000012
Decreased body height
Very rare (1-4%)HP:0004322
Deformity of face
Very rare (1-4%)HP:0001999
Epilepsy
Very rare (1-4%)HP:0001250
Quick Facts
- SNOMED CT
- 719209002
- UMLS CUI
- C1854488
- Fully Specified Name
- Spinocerebellar ataxia type 13 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.