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autosomal recessive spinocerebellar ataxia 15

ORPHA: 404499

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

human disease

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with autosomal recessive spinocerebellar ataxia 15, sourced from HPO and Orphanet clinical annotations.

Delayed speech and language developmentDysarthriaHyporeflexiaGait ataxiaLimb ataxiaDelayed gross motor developmentSaccadic smooth pursuit interruptionsIntellectual disabilitySeizureNystagmusPostural instability

Classification & Codes

Orphanet Code

ORPHA:404499
autosomal recessive spinocerebellar ataxia 15
OrphanetORPHA:404499
Treatments0 drug(s)
Symptoms on record11 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO