← Back to Conditions

Cerebellar ataxia Cayman type

disorder
SNOMED 717332007CUI C1832585

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 expressions
Always present (100%)HP:0000338
Degeneration of cerebellum
Always present (100%)HP:0001272
Fallen arches
Always present (100%)HP:0001763
Nonprogressive cerebellar ataxia
Very frequent (80-99%)HP:0002470
Squint
Very frequent (80-99%)HP:0000486
Cerebellar tremor
Frequent (30-79%)HP:0002080
Difficulty articulating speech
Frequent (30-79%)HP:0001260
Dystonic disease
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
Mental and motor retardation
Frequent (30-79%)HP:0001263
Muscle atrophy, neurogenic
Frequent (30-79%)HP:0003202
Slowness of movements
Frequent (30-79%)HP:0002067
Small cerebellum
Frequent (30-79%)HP:0001321
Abnormal retinal morphology
Excluded (<1%)HP:0000479
Muscular 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.