Overview
Spinocerebellar ataxia type 37 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.
Ataxia
Always present (100%)HP:0001251
Cogwheel rigidity
Very frequent (80-99%)HP:0002396
Difficulty articulating speech
Very frequent (80-99%)HP:0001260
Disconjugate eye movements
Very frequent (80-99%)HP:0000549
Falls
Very frequent (80-99%)HP:0002527
Abnormal vocalization
Frequent (30-79%)HP:0002167
Diffuse cerebellar atrophy
Frequent (30-79%)HP:0100275
Dysdiadochokinesis
Frequent (30-79%)HP:0002075
Explosive speech
Frequent (30-79%)HP:0002168
Gait disturbance
Frequent (30-79%)HP:0001288
Horizontal nystagmus
Frequent (30-79%)HP:0000666
Instability or lack of coordination of central trunk muscles
Frequent (30-79%)HP:0002078
Jerking
Frequent (30-79%)HP:0001336
Limb dysmetria
Frequent (30-79%)HP:0002406
Sensorineural deafness
Frequent (30-79%)HP:0000407
Sensory impairment
Frequent (30-79%)HP:0003474
Tremor
Frequent (30-79%)HP:0001337
Unsteady walk
Frequent (30-79%)HP:0002317
Vermian atrophy
Frequent (30-79%)HP:0006855
Deglutition disorder
Occasional (5-29%)HP:0002015
Involuntary, rapid, rhythmic eye movements
Occasional (5-29%)HP:0000639
Frequent falls
HP:0002359
Infratentorial atrophy
HP:0001272
Quick Facts
- SNOMED CT
- 719301002
- UMLS CUI
- C3889636
- Fully Specified Name
- Spinocerebellar ataxia type 37 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 23
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.