Autosomal recessive spastic paraplegia type 67

disorder

SNOMED 766767001CUI C4707829

Overview

Autosomal recessive spastic paraplegia type 67 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 myelination

Frequent (30-79%)HP:0012447

Abnormality of movement

Frequent (30-79%)HP:0100022

Absence of corpus callosum

Frequent (30-79%)HP:0001274

Cerebellar vermis aplasia or hypoplasia

Frequent (30-79%)HP:0006817

Cerebral cortex atrophy

Frequent (30-79%)HP:0002120

Extensor plantar responses

Frequent (30-79%)HP:0003487

Gait disturbance

Frequent (30-79%)HP:0001288

Increased reflexes

Frequent (30-79%)HP:0001347

Limb tremor

Frequent (30-79%)HP:0200085

Mental and motor retardation

Frequent (30-79%)HP:0001263

Mental retardation, mild

Frequent (30-79%)HP:0001256

Muscle atrophy, generalised

Frequent (30-79%)HP:0003700

Progressive spastic paraplegia

Frequent (30-79%)HP:0007020

Spastic walk

Frequent (30-79%)HP:0002064

Spasticity of lower limb

Frequent (30-79%)HP:0002061

Related Conditions

Complicated hereditary spastic paraplegia(parent)

Autosomal recessive hereditary spastic paraplegia(parent)

Quick Facts

SNOMED CT: 766767001
UMLS CUI: C4707829
Fully Specified Name: Autosomal recessive spastic paraplegia type 67 (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.