Overview
ITM2B-related cerebral amyloid angiopathy 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
Frequent (30-79%)HP:0011970
Deafness
Frequent (30-79%)HP:0000365
Lens opacities
Frequent (30-79%)HP:0000518
Leukoencephalopathy
Frequent (30-79%)HP:0002352
Progressive cerebellar ataxia
Frequent (30-79%)HP:0002073
Progressive dementia
Frequent (30-79%)HP:0000726
Spastic tetraparesis
Frequent (30-79%)HP:0001285
Tau-positive tangle
Frequent (30-79%)HP:0002185
Related Conditions
Familial dementia British type(child)
Familial dementia Danish type(child)
Autosomal dominant hereditary disorder(parent)
Chronic disorder of cardiovascular system(parent)
Cerebral amyloid angiopathy(parent)
Cardiovascular system hereditary disorder(parent)
Hereditary amyloidosis(parent)
Chronic organic mental disorder(parent)
Dementia(parent)
Vascular disease(parent)
Hereditary disorder of nervous system(parent)
Quick Facts
- SNOMED CT
- 1187126002
- UMLS CUI
- C5568806
- Fully Specified Name
- Integral membrane protein 2B related amyloidosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 8
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.