Overview
Spinocerebellar ataxia type 4 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.
Absent Achilles reflex
Very frequent (80-99%)HP:0003438
Impaired proprioception
Very frequent (80-99%)HP:0010831
Impaired vibratory sensation
Very frequent (80-99%)HP:0002495
Loss of tactile sensation
Very frequent (80-99%)HP:0010830
Ataxia
Frequent (30-79%)HP:0001251
Difficulty articulating speech
Frequent (30-79%)HP:0001260
Gait disturbance
Frequent (30-79%)HP:0001288
Progressive degeneration of movement
Frequent (30-79%)HP:0002333
Absent tendon reflexes
Occasional (5-29%)HP:0001284
Distal motor neuropathy
Occasional (5-29%)HP:0007002
Peripheral neuropathy
Occasional (5-29%)HP:0009830
Sensory axonal neuropathy
Occasional (5-29%)HP:0003390
Atrophic cerebellum
HP:0001272
Extensor plantar responses
HP:0003487
Hyporeflexia
HP:0001265
Impaired smooth pursuit
HP:0007772
Loss of distal sensation
HP:0002936
Progressive cerebellar ataxia
HP:0002073
Sensory neuropathy
HP:0000763
Uncoordinated limb movement
HP:0002406
Quick Facts
- SNOMED CT
- 715755008
- UMLS CUI
- C0752122
- Fully Specified Name
- Spinocerebellar ataxia type 4 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 20
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.