Familial cerebral saccular aneurysm

disorder

SNOMED 703226008CUI C3839866

Overview

Familial cerebral saccular aneurysm 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.

Cerebral saccular aneurysm

Always present (100%)HP:0007029

Abnormal circle of Willis morphology

Frequent (30-79%)HP:0012518

Abnormality of brainstem morphology

Frequent (30-79%)HP:0002363

Epilepsy

Frequent (30-79%)HP:0001250

Hemiparesis

Frequent (30-79%)HP:0001269

High blood pressure

Frequent (30-79%)HP:0000822

Partial loss of field of vision

Frequent (30-79%)HP:0001123

Plaque build-up in arteries

Frequent (30-79%)HP:0002621

Transient ischemic attacks

Frequent (30-79%)HP:0002326

Aortic dissection

Occasional (5-29%)HP:0002647

Cerebral softening

Occasional (5-29%)HP:0040197

Increased aortic root diameter

Occasional (5-29%)HP:0002616

Intracranial haemorrhage

Occasional (5-29%)HP:0002170

Oculomotor neuropathy

Occasional (5-29%)HP:0012246

Subarachnoid hemorrhage

Occasional (5-29%)HP:0002138

Related Conditions

Berry aneurysm(parent)

Familial disease(parent)

Autosomal hereditary disorder(parent)

Cardiovascular system hereditary disorder(parent)

Quick Facts

SNOMED CT: 703226008
UMLS CUI: C3839866
Fully Specified Name: Familial cerebral saccular aneurysm (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

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.