Overview
Corneal cerebellar syndrome 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
Frequent (30-79%)HP:0001251
Corneal dystrophy
Frequent (30-79%)HP:0001131
Corneal opacity
Frequent (30-79%)HP:0007957
Dorsal column degeneration
Frequent (30-79%)HP:0007006
Impaired vision
Frequent (30-79%)HP:0000505
Moderate mental retardation
Frequent (30-79%)HP:0002342
Progressive cerebellar ataxia
Frequent (30-79%)HP:0002073
Pyramidal tract dysfunction
Frequent (30-79%)HP:0002493
Spinocerebellar tract degeneration
Frequent (30-79%)HP:0002503
Cloudy cornea
HP:0007759
Corneal stromal edema
HP:0012040
Mental deficiency
HP:0001249
Severely impaired vision
HP:0001141
Quick Facts
- SNOMED CT
- 720750004
- UMLS CUI
- C1849087
- Fully Specified Name
- Spinocerebellar degeneration and corneal dystrophy syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 13
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.