Hereditary sensory autonomic neuropathy type IC

disorder

SNOMED 860814001CUI C3150896

Overview

Hereditary sensory autonomic neuropathy type IC 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 muscle weakness in lower limbs

Always present (100%)HP:0009053

Distal sensory loss, especially vibratory sense

Always present (100%)HP:0002166

Distal upper limb muscle weakness

Always present (100%)HP:0008959

Hyporeflexia of lower limbs

Always present (100%)HP:0002600

Impaired pain sensation

Always present (100%)HP:0007328

Loss of distal sensation

Always present (100%)HP:0002936

Nerve damage causing decreased feeling and movement

Always present (100%)HP:0007141

Upper limb hyperreflexia

Always present (100%)HP:0007350

Weakness of outermost muscles

Very frequent (80-99%)HP:0002460

Hand tingling

Frequent (30-79%)HP:0033660

Open skin sore

Frequent (30-79%)HP:0200042

Osteomyelitis

Frequent (30-79%)HP:0002754

Autoamputation of digits

Occasional (5-29%)HP:0007460

Distal sensory impairment of all modalities

Occasional (5-29%)HP:0003409

Dysesthesia

Occasional (5-29%)HP:0012534

Sweating dysfunction

Occasional (5-29%)HP:0000970

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary sensory and autonomic neuropathy type I(parent)

Quick Facts

SNOMED CT: 860814001
UMLS CUI: C3150896
Fully Specified Name: Hereditary sensory autonomic neuropathy type IC (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 17

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.