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Autosomal dominant spastic paraplegia type 29
disorderSNOMED 733029008CUI C1857855
Overview
Autosomal dominant spastic paraplegia 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.
Extensor plantar responses
Very frequent (80-99%)HP:0003487
Lower limb hyperreflexia
Very frequent (80-99%)HP:0002395
Cavus foot
Frequent (30-79%)HP:0001761
Deafness
Frequent (30-79%)HP:0000365
Hernia
Frequent (30-79%)HP:0100790
High blood bilirubin levels
Frequent (30-79%)HP:0002904
Stomach hernia
Frequent (30-79%)HP:0002036
Abnormality of the lower urinary tract
Occasional (5-29%)HP:0010936
Clonus
Occasional (5-29%)HP:0002169
Impaired vibratory sensation
Occasional (5-29%)HP:0002495
Upper limb hyperreflexia
Occasional (5-29%)HP:0007350
Abnormal rectum morphology
Very rare (1-4%)HP:0002034
Impaired proprioception
Very rare (1-4%)HP:0010831
Seizures
Very rare (1-4%)HP:0001250
Hyperactive behaviour
HP:0000752
Hyperbilirubinemia, neonatal
HP:0003265
Increased reflexes
HP:0001347
Nocturia
HP:0000017
Sensorineural deafness
HP:0000407
Spastic paraplegia
HP:0001258
Spasticity of lower limb
HP:0002061
Upper extremity spasticity
HP:0006986
Urinary hesitancy
HP:0000019
Urinary incontinence
HP:0000020
Urinary urgency
HP:0000012
Vomiting
HP:0002013
Quick Facts
- SNOMED CT
- 733029008
- UMLS CUI
- C1857855
- Fully Specified Name
- Autosomal dominant spastic paraplegia type 29 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 26
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.