Hereditary cerebral amyloid angiopathy, Icelandic type

disorder

SNOMED 45639009CUI C1527338

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.

Cerebral amyloid angiopathy

Very frequent (80-99%)HP:0011970

Cerebral vascular events

Very frequent (80-99%)HP:0001297

Amyloidosis

Frequent (30-79%)HP:0011034

Cerebral cortex atrophy

Frequent (30-79%)HP:0002120

Dilated cerebral perivascular spaces

Frequent (30-79%)HP:0012520

Epilepsy

Frequent (30-79%)HP:0001250

Headache

Frequent (30-79%)HP:0002315

Subarachnoid hemorrhage

Frequent (30-79%)HP:0002138

Worsening neurological symptoms

Frequent (30-79%)HP:0002344

Cerebral cortical microinfarct

Occasional (5-29%)HP:0025714

Cerebrospinal fluid pleocytosis

Occasional (5-29%)HP:0012229

Elevated csf protein

Occasional (5-29%)HP:0002922

Hyperintensity of cerebral white matter on MRI

Occasional (5-29%)HP:0030890

Progressive dementia

Occasional (5-29%)HP:0000726

Generalised amyloid deposition

HP:0003216

Hemorrhagic stroke

HP:0001342

Intracranial haemorrhage

HP:0002170

Related Conditions

Hereditary cerebral hemorrhage with amyloidosis(parent)

Cerebral hemorrhage(parent)

Chronic brain syndrome(parent)

Quick Facts

SNOMED CT: 45639009
UMLS CUI: C1527338
Fully Specified Name: Hereditary cerebral amyloid angiopathy, Icelandic type (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.