Autosomal recessive spastic paraplegia type 63

disorder

SNOMED 726610000CUI C3810295

Overview

Autosomal recessive spastic paraplegia type 63 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.

Delayed ability to walk

Always present (100%)HP:0031936

Extensor plantar responses

Always present (100%)HP:0003487

Gait disturbance

Always present (100%)HP:0001288

Clonus

Frequent (30-79%)HP:0002169

Decreased body height

Frequent (30-79%)HP:0004322

Decreased body weight

Frequent (30-79%)HP:0004325

Decreased vibration sense in feet

Frequent (30-79%)HP:0006938

Delayed gross motor development

Frequent (30-79%)HP:0002194

Hypertonia

Frequent (30-79%)HP:0001276

Hypoplasia of corpus callosum

Frequent (30-79%)HP:0002079

Increased reflexes

Frequent (30-79%)HP:0001347

Involuntary muscle stiffness, contraction, or spasm

Frequent (30-79%)HP:0001257

Muscle degeneration

Frequent (30-79%)HP:0003202

Scissor gait

Frequent (30-79%)HP:0012407

Abnormality of the periventricular white matter

Occasional (5-29%)HP:0002518

Poor school performance

Excluded (<1%)HP:0001249

Spastic paraplegia

HP:0001258

Related Conditions

Complicated hereditary spastic paraplegia(parent)

Autosomal recessive hereditary spastic paraplegia(parent)

Quick Facts

SNOMED CT: 726610000
UMLS CUI: C3810295
Fully Specified Name: Autosomal recessive spastic paraplegia type 63 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 17

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.