Hereditary sensory autonomic neuropathy type IIA

disorder

SNOMED 860809000CUI C2752089

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Absent deep tendon reflexes

HP:0001284

Acral ulceration

HP:0006121

Acroosteolysis of feet

HP:0001842

Autoamputation of digits

HP:0007460

Decreased nerve conduction velocity

HP:0000762

Decreased number of large and small myelinated fibres

HP:0003380

Decreased sensory NCV

HP:0003448

Decreased taste sensation

HP:0000224

Episodic hyperhidrosis

HP:0001069

Feeding difficulties in infancy

HP:0008872

Gastroesophageal reflux disease

HP:0002020

Generalised decreased muscle tone

HP:0001290

Hyporeflexia

HP:0001265

Laboratory abnormality

HP:0001939

Muscular hypotonia

HP:0001252

Neuropathy

HP:0009830

Osteolytic defects of the phalanges of the hand

HP:0009771

Painless fractures due to injury

HP:0002661

Paronychia

HP:0001818

Reduced corneal reflex

HP:0008000

Sweating dysfunction

HP:0000970

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Hereditary sensory and autonomic neuropathy type II(parent)

Quick Facts

SNOMED CT: 860809000
UMLS CUI: C2752089
Fully Specified Name: Hereditary sensory autonomic neuropathy type IIA (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 21

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.