SCA46 - spinocerebellar ataxia type 46

disorder

SNOMED 1279839002CUI C4540404

Overview

SCA46 - spinocerebellar ataxia type 46 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.

Abnormal finger chase test

HP:0001310

Appendicular ataxia

HP:0002070

Difficulty articulating speech

HP:0001260

Inability to coordinate movements when walking

HP:0002066

Infratentorial atrophy

HP:0001272

Involuntary, rapid, rhythmic eye movements

HP:0000639

Jerky ocular pursuit movements

HP:0008003

Peripheral sensory axonal neuropathy

HP:0003390

Positive Romberg sign

HP:0002403

Slow visual tracking

HP:0000514

Related Conditions

Autosomal dominant hereditary disorder(parent)

Spinocerebellar ataxia(parent)

Chronic brain syndrome(parent)

Chronic disorder of spinal cord(parent)

Quick Facts

SNOMED CT: 1279839002
UMLS CUI: C4540404
Fully Specified Name: Spinocerebellar ataxia type 46 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.