Progressive polyneuropathy with bilateral striatal necrosis

disorder

SNOMED 771305006CUI C3150973

Overview

Progressive polyneuropathy with bilateral striatal necrosis 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.

Gait disturbance

Always present (100%)HP:0001288

Increased CSF lactic acid

Always present (100%)HP:0002490

Weakness of outermost muscles

Always present (100%)HP:0002460

Contractures of the joints of the lower limbs

Frequent (30-79%)HP:0005750

Muscle wasting

Frequent (30-79%)HP:0003202

Loss of distal sensation

Occasional (5-29%)HP:0002936

Axonal neuropathy

HP:0003477

Foot, talipes equinovarus

HP:0001762

Hyporeflexia

HP:0001265

Inactivity

HP:0001254

Muscle weakness

HP:0001324

Paralysis

HP:0003470

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Polyneuropathy(parent)

Chronic brain syndrome(parent)

Brain tissue injury(parent)

Chronic metabolic disease(parent)

Hereditary disorder of nervous system(parent)

Metabolic encephalopathy(parent)

Lesion of brain(parent)

Peripheral nerve injury(parent)

Tissue necrosis(parent)

Abnormal corpus striatum morphology(parent)

Quick Facts

SNOMED CT: 771305006
UMLS CUI: C3150973
Fully Specified Name: Progressive polyneuropathy with bilateral striatal necrosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 12

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.