Palmoplantar keratoderma, spastic paralysis syndrome

disorder

SNOMED 785725008CUI C2931828

Overview

Palmoplantar keratoderma, spastic paralysis syndrome 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 electromyography finding

Very frequent (80-99%)HP:0003457

Abnormal toenail morphology

Very frequent (80-99%)HP:0008388

Abnormality of the fingernails

Very frequent (80-99%)HP:0001231

Absence of pain sensation

Very frequent (80-99%)HP:0007021

Cavus foot

Very frequent (80-99%)HP:0001761

Gait disturbance

Very frequent (80-99%)HP:0001288

Keratoderma

Very frequent (80-99%)HP:0000982

Muscle flaccidity

Very frequent (80-99%)HP:0010547

Neuropathy

Very frequent (80-99%)HP:0009830

Pachydermia

Very frequent (80-99%)HP:0001072

Involuntary muscle stiffness, contraction, or spasm

Frequent (30-79%)HP:0001257

Paralysis on one side of body

Frequent (30-79%)HP:0002301

Related Conditions

Autosomal dominant hereditary disorder(parent)

Punctate palmoplantar keratoderma(parent)

Inherited disorder of keratinization(parent)

Quick Facts

SNOMED CT: 785725008
UMLS CUI: C2931828
Fully Specified Name: Palmoplantar keratoderma, spastic paralysis syndrome (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.