Spinocerebellar ataxia type 41

disorder

SNOMED 1208512000CUI C4225158

Overview

Spinocerebellar ataxia type 41 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.

Unsteady walk

Always present (100%)HP:0002317

Imbalance

Frequent (30-79%)HP:0002172

Inability to coordinate movements when walking

Frequent (30-79%)HP:0002066

Vermian atrophy

Frequent (30-79%)HP:0006855

Ataxia

HP:0001251

Degeneration of cerebellum

HP:0001272

Related Conditions

Autosomal dominant hereditary disorder(parent)

Spinocerebellar ataxia(parent)

Chronic brain syndrome(parent)

Chronic disorder of spinal cord(parent)

Quick Facts

SNOMED CT: 1208512000
UMLS CUI: C4225158
Fully Specified Name: Spinocerebellar ataxia type 41 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 6

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.