Hereditary sensory autonomic neuropathy type IA

disorder

SNOMED 860813007CUI C5235211

Overview

Hereditary sensory autonomic neuropathy type IA 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.

Decreased motor nerve conduction velocity

Always present (100%)HP:0003431

Distal limb muscle weakness due to peripheral neuropathy

Always present (100%)HP:0002460

Frequent falls

Always present (100%)HP:0002359

Impaired distal proprioception

Always present (100%)HP:0006858

Impaired distal tactile sensation

Always present (100%)HP:0006937

Lens opacities

Always present (100%)HP:0000518

Muscle wasting

Always present (100%)HP:0003202

Tongue fasciculations/fibrillations

Always present (100%)HP:0001308

tremors in hands

Always present (100%)HP:0002378

Absent deep tendon reflexes

HP:0001284

Acral ulceration

HP:0006121

Autoamputation of foot

HP:0001868

Bone infection

HP:0002754

Cavus foot

HP:0001761

Chronic axonal neuropathy

HP:0007267

Decreased sensory NCV

HP:0003448

Distal sensory impairment of all modalities

HP:0003409

Foot osteomyelitis

HP:0001886

Hyporeflexia

HP:0001265

Loss of distal sensation

HP:0002936

Loss of large myelinated fibres

HP:0003387

Sensorineural deafness

HP:0000407

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary sensory and autonomic neuropathy type I(parent)

Quick Facts

SNOMED CT: 860813007
UMLS CUI: C5235211
Fully Specified Name: Hereditary sensory autonomic neuropathy type IA (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 22

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.