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Spinocerebellar ataxia type 29

disorder
SNOMED 715825009CUI C1861732

Overview

Spinocerebellar ataxia type 29 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 eye contact
Always present (100%)HP:0034435
Arc de cercle
Always present (100%)HP:0002179
Ataxic tremor
Always present (100%)HP:0002345
Atria septal defect
Always present (100%)HP:0001631
Bilateral facial muscle weakness
Always present (100%)HP:0430025
Brisk deep tendon reflexes
Always present (100%)HP:0001348
Bruxism
Always present (100%)HP:0003763
Cardiac anomaly
Always present (100%)HP:0001627
Cerebellar ataxia associated with quadrupedal gait
Always present (100%)HP:0009878
Clumsy tandem walking
Always present (100%)HP:0031629
Congenital horizontal nystagmus
Always present (100%)HP:0007859
Congenital hypotonia
Always present (100%)HP:0001319
Convergent squint
Always present (100%)HP:0020045
Cryptorchidism
Always present (100%)HP:0000028
CVI
Always present (100%)HP:0100704
Decreased body height
Always present (100%)HP:0004322
Degeneration of cerebrum
Always present (100%)HP:0002059
Delayed ability to crawl
Always present (100%)HP:0033128
Delayed ability to sit
Always present (100%)HP:0025336
Delayed ability to stand
Always present (100%)HP:0025335
Delayed ability to walk with support
Always present (100%)HP:0033257
Depressed philtrum
Always present (100%)HP:0002002
Difficulty making arithmetical calculations
Always present (100%)HP:0002442
Distortion of face
Always present (100%)HP:0001999
Divergent strabismus
Always present (100%)HP:0020049
Dystonic movements
Always present (100%)HP:0001332
Echologia
Always present (100%)HP:0010529
Electrical status epilepticus during slow-wave sleep
Always present (100%)HP:0031491
Elf-like facial features
Always present (100%)HP:0004428
Enuresis
Always present (100%)HP:0000805

Quick Facts

SNOMED CT
715825009
UMLS CUI
C1861732
Fully Specified Name
Spinocerebellar ataxia type 29 (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
30
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.