Cerebral arteriovenous malformation

disorder

SNOMED 234142008CUI C0917804

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.

Abnormality of the cerebral blood vessels

Very frequent (80-99%)HP:0100659

Peripheral arteriovenous fistula

Very frequent (80-99%)HP:0100784

Visceral angiomatosis

Very frequent (80-99%)HP:0100761

Epilepsy

Frequent (30-79%)HP:0001250

Hemorrhagic stroke

Frequent (30-79%)HP:0001342

Intellectual impairment

Frequent (30-79%)HP:0100543

Intraventricular hemorrhage

Frequent (30-79%)HP:0030746

Memory impairment

Frequent (30-79%)HP:0002354

Poor vision

Frequent (30-79%)HP:0000505

Headache

Occasional (5-29%)HP:0002315

Reduced attention regulation

Occasional (5-29%)HP:5200044

Cerebral AV malformation

HP:0002408

Related Conditions

AVM - Ruptured cerebral arteriovenous malformation(child)

Cerebrofacial arteriovenous metameric syndrome(child)

Lymphedema and cerebral arteriovenous anomaly syndrome(child)

Congenital arteriovenous malformation(parent)

Intracranial vascular malformation(parent)

Quick Facts

SNOMED CT: 234142008
UMLS CUI: C0917804
Fully Specified Name: Cerebral arteriovenous malformation (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.