Mitchell syndrome

disorder

SNOMED 1300194008CUI C5394554

Overview

Mitchell 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.

Areflexia in lower limbs

HP:0002522

Autonomic dysregulation

HP:0012332

Clumsiness

HP:0002312

Cortical white matter abnormalities seen on MRI

HP:0002500

Deglutition disorder

HP:0002015

Encephalopathy

HP:0001298

Epilepsy

HP:0001250

Gait disturbance

HP:0001288

Hyporeflexia of upper limbs

HP:0012391

Limb muscle weakness

HP:0003690

No speech development

HP:0001344

Respiratory failure due to muscle weakness

HP:0002747

Sensory axonal neuropathy

HP:0003390

Related Conditions

Autosomal dominant hereditary disorder(parent)

Chronic nervous system disease(parent)

Hearing loss associated with syndrome(parent)

Demyelinating polyneuropathy(parent)

Mixed sensory-motor polyneuropathy(parent)

Hereditary disorder of nervous system(parent)

Hereditary hearing loss(parent)

Quick Facts

SNOMED CT: 1300194008
UMLS CUI: C5394554
Fully Specified Name: Mitchell syndrome (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.