Overview
Cerebellar ataxia Cayman type 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
Decreased facial muscle movement
Always present (100%)HP:0000338
Degeneration of cerebellum
Always present (100%)HP:0001272
Dropped arches
Always present (100%)HP:0001763
Nonprogressive cerebellar ataxia
Very frequent (80-99%)HP:0002470
Squint
Very frequent (80-99%)HP:0000486
Difficulty articulating speech
Frequent (30-79%)HP:0001260
Dystonic movements
Frequent (30-79%)HP:0001332
Generalised decreased muscle tone
Frequent (30-79%)HP:0001290
Inability to coordinate movements when walking
Frequent (30-79%)HP:0002066
Instability or lack of coordination of central trunk muscles
Frequent (30-79%)HP:0002078
Involuntary, rapid, rhythmic eye movements
Frequent (30-79%)HP:0000639
Muscle atrophy, neurogenic
Frequent (30-79%)HP:0003202
Psychomotor development deficiency
Frequent (30-79%)HP:0001263
Slowness of movements
Frequent (30-79%)HP:0002067
Small cerebellum
Frequent (30-79%)HP:0001321
Terminal tremor
Frequent (30-79%)HP:0002080
Abnormal retinal morphology
Excluded (<1%)HP:0000479
Peripheral hypotonia
HP:0001252
Wide based walk
HP:0002136
Quick Facts
- SNOMED CT
- 717332007
- UMLS CUI
- C1832585
- Fully Specified Name
- Cerebellar ataxia Cayman type (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.