Hereditary cerebral amyloid angiopathy, Dutch type

disorder

SNOMED 56453003CUI C2931672

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.

Cerebellar haemorrhage

Always present (100%)HP:0011695

Behavioural/Psychiatric abnormality

Very frequent (80-99%)HP:0000708

Cerebral hemorrhage

Very frequent (80-99%)HP:0001342

Cerebral vascular events

Very frequent (80-99%)HP:0001297

Headache

Very frequent (80-99%)HP:0002315

Intellectual deterioration

Very frequent (80-99%)HP:0001268

Progressive dementia

Very frequent (80-99%)HP:0000726

Abnormal deposits of calcium in the brain

Frequent (30-79%)HP:0002514

Cerebral amyloid angiopathy

Frequent (30-79%)HP:0011970

Recurrent cerebral hemorrhage

Frequent (30-79%)HP:0004968

Seizures

Frequent (30-79%)HP:0001250

Paresthesia

Occasional (5-29%)HP:0003401

Subarachnoid hemorrhage

Occasional (5-29%)HP:0002138

Brain ischemia

HP:0002637

Tortuous cerebral arteries

HP:0004938

Related Conditions

Hereditary cerebral hemorrhage with amyloidosis(parent)

Quick Facts

SNOMED CT: 56453003
UMLS CUI: C2931672
Fully Specified Name: Hereditary cerebral amyloid angiopathy, Dutch type (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.