Autosomal recessive spastic paraplegia type 61

disorder

SNOMED 726611001CUI C3810294

Overview

Autosomal recessive spastic paraplegia type 61 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.

Absent Achilles reflex

Always present (100%)HP:0003438

Inability to walk

Always present (100%)HP:0002540

Sensory neuropathy

Always present (100%)HP:0000763

Abnormality of the calcaneal tendon

Frequent (30-79%)HP:0005109

Abnormality of the knee

Frequent (30-79%)HP:0002815

Gait disturbance

Frequent (30-79%)HP:0001288

Involuntary muscle stiffness, contraction, or spasm

Frequent (30-79%)HP:0001257

Overactive knee reflex

Frequent (30-79%)HP:0007083

Peripheral motor neuropathy

Frequent (30-79%)HP:0007178

Peripheral nerve disease

Frequent (30-79%)HP:0001271

Scissor gait

Frequent (30-79%)HP:0012407

Nonprogressive mental retardation

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: 726611001
UMLS CUI: C3810294
Fully Specified Name: Autosomal recessive spastic paraplegia type 61 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

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.