Autosomal recessive spastic paraplegia type 64

disorder

SNOMED 726609005CUI C3810289

Overview

Autosomal recessive spastic paraplegia type 64 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.

Spastic paraplegia

Always present (100%)HP:0001258

Decreased size of cranium

Frequent (30-79%)HP:0000252

Delayed puberty

Frequent (30-79%)HP:0000823

Difficulty articulating speech

Frequent (30-79%)HP:0001260

Gait disturbance

Frequent (30-79%)HP:0001288

Involuntary muscle stiffness, contraction, or spasm

Frequent (30-79%)HP:0001257

Mental retardation, borderline

Frequent (30-79%)HP:0006889

Abnormality of the cerebral white matter

Occasional (5-29%)HP:0002500

Absent tendon reflexes

Occasional (5-29%)HP:0001284

Cataract, congenital

Occasional (5-29%)HP:0000519

Foot, talipes equinovarus

Occasional (5-29%)HP:0001762

Moderate mental retardation

HP:0002342

Muscle wasting

HP:0003202

Nonprogressive mental retardation

HP:0001249

physical aggression

HP:0000718

Related Conditions

Complicated hereditary spastic paraplegia(parent)

Autosomal recessive hereditary spastic paraplegia(parent)

Quick Facts

SNOMED CT: 726609005
UMLS CUI: C3810289
Fully Specified Name: Autosomal recessive spastic paraplegia type 64 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

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.