Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy

disorder

SNOMED 390936003CUI C0751587

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.

Abulia

Always present (100%)HP:0012671

Perseverative behaviour

Always present (100%)HP:0030223

Personality changes

Always present (100%)HP:0000751

Psychosis

Always present (100%)HP:0000709

Cortical white matter abnormalities seen on MRI

Very frequent (80-99%)HP:0002500

Lacunar stroke

Very frequent (80-99%)HP:0032325

Leukoencephalopathy

Very frequent (80-99%)HP:0002352

Multifocal hyperintensity of cerebral white matter on MRI

Very frequent (80-99%)HP:0040329

Brain ischemia

Frequent (30-79%)HP:0002637

Cerebral vascular events

Frequent (30-79%)HP:0001297

Cognitive deficits

Frequent (30-79%)HP:0100543

Emotional lability

Frequent (30-79%)HP:0000712

Hemiparesis

Frequent (30-79%)HP:0001269

Lack of feeling, emotion, interest

Frequent (30-79%)HP:0000741

Migraine headache

Frequent (30-79%)HP:0002076

Migraine with aura

Frequent (30-79%)HP:0002077

Transient ischemic attacks

Frequent (30-79%)HP:0002326

Urinary incontinence

Frequent (30-79%)HP:0000020

Anxiety disease

Occasional (5-29%)HP:0000739

Arterial stenosis

Occasional (5-29%)HP:0100545

Brain wasting

Occasional (5-29%)HP:0012444

Confusion

Occasional (5-29%)HP:0001289

Deglutition disorder

Occasional (5-29%)HP:0002015

Depression

Occasional (5-29%)HP:0000716

Diabetes mellitus

Occasional (5-29%)HP:0000819

Difficulty articulating speech

Occasional (5-29%)HP:0001260

Encephalopathy

Occasional (5-29%)HP:0001298

Gait disturbance

Occasional (5-29%)HP:0001288

Hemorrhagic stroke

Occasional (5-29%)HP:0001342

High blood pressure

Occasional (5-29%)HP:0000822

Related Conditions

White matter disorder co-occurrent and due to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy(child)

Cerebrovascular disease(parent)

Quick Facts

SNOMED CT: 390936003
UMLS CUI: C0751587
Fully Specified Name: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.