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Hereditary cerebral hemorrhage with amyloidosis

disorder
SNOMED 724357007CUI C1510489

Overview

Hereditary cerebral hemorrhage with amyloidosis 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 amyloid angiopathy
Very frequent (80-99%)HP:0011970
Cerebral cortex atrophy
Frequent (30-79%)HP:0002120
Dilated Virchow-Robin spaces
Frequent (30-79%)HP:0012520
Headache
Frequent (30-79%)HP:0002315
Seizures
Frequent (30-79%)HP:0001250
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
Cerebral vascular events
HP:0001297
Generalised amyloid deposition
HP:0003216
Hemorrhagic stroke
HP:0001342
Intracranial haemorrhage
HP:0002170

Quick Facts

SNOMED CT
724357007
UMLS CUI
C1510489
Fully Specified Name
Hereditary cerebral hemorrhage with amyloidosis (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
16
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.