Overview
X-linked non progressive cerebellar ataxia 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.
Nonprogressive cerebellar ataxia
Very frequent (80-99%)HP:0002470
Action tremor
Frequent (30-79%)HP:0002345
Cerebellar vermis hypoplasia
Frequent (30-79%)HP:0001320
Clumsiness
Frequent (30-79%)HP:0002312
Frequent falls
Frequent (30-79%)HP:0002359
Generalized low muscle tone in neonate
Frequent (30-79%)HP:0008935
Instability or lack of coordination of central trunk muscles
Frequent (30-79%)HP:0002078
No development of motor milestones
Frequent (30-79%)HP:0001270
Rigid dysarthria
Frequent (30-79%)HP:0002464
Saccadic slow pursuit
Frequent (30-79%)HP:0001152
Small cerebellum
Frequent (30-79%)HP:0001321
Squint
Frequent (30-79%)HP:0000486
Terminal tremor
Frequent (30-79%)HP:0002080
Unsteady walk
Frequent (30-79%)HP:0002317
Quick Facts
- SNOMED CT
- 766818009
- UMLS CUI
- C4707849
- Fully Specified Name
- X-linked non progressive cerebellar ataxia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 14
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.