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CARASIL syndrome

disorder
SNOMED 703219008CUI C1838577

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.

Abnormal finger chase test
Always present (100%)HP:0001310
Anal incontinence
Always present (100%)HP:0002607
Arteriosclerosis of small cerebral arteries
Always present (100%)HP:0004931
Brain degeneration
Always present (100%)HP:0012444
Carotid artery stenosis
Always present (100%)HP:0100546
Delusions
Always present (100%)HP:0000746
Difficulty finding words
Always present (100%)HP:0002381
Diffuse white matter abnormalities
Always present (100%)HP:0007204
Excessive, persistent worry and fear
Always present (100%)HP:0000739
Gait apraxia
Always present (100%)HP:0010521
Lacunar stroke
Always present (100%)HP:0032325
Leukoencephalopathy
Always present (100%)HP:0002352
Pseudobulbar symptoms
Always present (100%)HP:0002200
Sensory hallucination
Always present (100%)HP:0000738
Transient ischemic attacks
Always present (100%)HP:0002326
Urinary incontinence
Always present (100%)HP:0000020
Hair loss
Very frequent (80-99%)HP:0001596
Back pain
Frequent (30-79%)HP:0003418
Behavioral changes
Frequent (30-79%)HP:0000708
Cervical spondylosis
Frequent (30-79%)HP:0008480
Deep cerebral white matter hyperintensities
Frequent (30-79%)HP:0030892
Gait disturbance
Frequent (30-79%)HP:0001288
Hardened artery wall
Frequent (30-79%)HP:0002634
Intellectual impairment
Frequent (30-79%)HP:0100543
Involuntary muscle stiffness, contraction, or spasm
Frequent (30-79%)HP:0001257
Localized osteoporosis
Frequent (30-79%)HP:0040161
Lower limb pain
Frequent (30-79%)HP:0012514
Pseudobulbar palsy
Frequent (30-79%)HP:0007024
Spastic ataxia
Frequent (30-79%)HP:0002497
Stroke-like episode
Frequent (30-79%)HP:0002401

Quick Facts

SNOMED CT
703219008
UMLS CUI
C1838577
Fully Specified Name
Cerebral autosomal recessive 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.