Overview
Spinocerebellar ataxia type 14 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.
Inability to coordinate movements when walking
Very frequent (80-99%)HP:0002066
Abnormality of the calcaneal tendon
Frequent (30-79%)HP:0005109
Appendicular ataxia
Frequent (30-79%)HP:0002070
Generalised decreased muscle tone
Frequent (30-79%)HP:0001290
Progressive cerebellar ataxia
Frequent (30-79%)HP:0002073
Vermian atrophy
Frequent (30-79%)HP:0006855
Difficulty articulating speech
Occasional (5-29%)HP:0001260
Gaze-evoked nystagmus
Occasional (5-29%)HP:0000640
Hyporeflexia of lower limbs
Occasional (5-29%)HP:0002600
Intellectual impairment
Occasional (5-29%)HP:0100543
Involuntary jerking movements
Occasional (5-29%)HP:0001336
Muscle rigidity
Occasional (5-29%)HP:0002063
Saccadic slow pursuit
Occasional (5-29%)HP:0001152
Sensory impairment
Occasional (5-29%)HP:0003474
Tremor
Occasional (5-29%)HP:0001337
Abnormal finger-nose-finger test
HP:0001310
Childhood attention deficit/hyperactivity disorder
HP:0007018
Decreased vibration sense in feet
HP:0006938
Degeneration of cerebellum
HP:0001272
Deglutition disorder
HP:0002015
Depressive episode
HP:0000716
Focal dystonia
HP:0004373
Increased reflexes
HP:0001347
Intellectual deterioration
HP:0001268
Involuntary facial quivering
HP:0000317
Involuntary, rapid, rhythmic eye movements
HP:0000639
Memory impairment
HP:0002354
Quick Facts
- SNOMED CT
- 719210007
- UMLS CUI
- C1854369
- Fully Specified Name
- Spinocerebellar ataxia type 14 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 27
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.