Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations

disorder

SNOMED 783787000CUI C1860518

Overview

Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations 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.

Abnormality of retina blood vessels

Very frequent (80-99%)HP:0008046

Abnormality of the cerebral white matter

Very frequent (80-99%)HP:0002500

Raynaud phenomenon

Very frequent (80-99%)HP:0030880

Abnormality of liver blood vessels

Frequent (30-79%)HP:0006707

Brain imaging abnormality

Frequent (30-79%)HP:0410263

Cognitive deficits

Frequent (30-79%)HP:0100543

Elevated alkaline phosphatase

Frequent (30-79%)HP:0003155

Elevated gamma-glutamyltransferase level

Frequent (30-79%)HP:0030948

High blood pressure

Frequent (30-79%)HP:0000822

Increased creatinine

Frequent (30-79%)HP:0003259

Intermittent migraine headaches

Frequent (30-79%)HP:0002076

Kidney disease

Frequent (30-79%)HP:0000112

Mild hypothyroidism

Frequent (30-79%)HP:0008223

Nodular regenerative hyperplasia of liver

Frequent (30-79%)HP:0011954

Normochromic anaemia

Frequent (30-79%)HP:0001895

Normocytic anemia

Frequent (30-79%)HP:0001897

Progressive dementia

Frequent (30-79%)HP:0000726

Renal glomerular fibrosis

Frequent (30-79%)HP:0000096

Abnormal deposits of calcium in the brain

Occasional (5-29%)HP:0002514

Depression

Occasional (5-29%)HP:0000716

Difficulty finding words

Occasional (5-29%)HP:0002381

Disease of the heart muscle

Occasional (5-29%)HP:0001638

Excessive, persistent worry and fear

Occasional (5-29%)HP:0000739

Focal hyperintensity of cerebral white matter on MRI

Occasional (5-29%)HP:0040328

Focal hypointensity of cerebral white matter on MRI

Occasional (5-29%)HP:0040331

Focal sensory seizure with somatosensory features

Occasional (5-29%)HP:0011163

Gastrointestinal haemorrhage

Occasional (5-29%)HP:0002239

Generalised-onset seizure

Occasional (5-29%)HP:0002197

Glaucoma

Occasional (5-29%)HP:0000501

Hemianopia

Occasional (5-29%)HP:0012377

Related Conditions

Hereditary disorder of the visual system(parent)

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of immune system(parent)

Cerebral small vessel disease(parent)

Hereditary disorder of nervous system(parent)

Cardiovascular system hereditary disorder(parent)

Chronic disorder of cardiovascular system(parent)

Chronic brain syndrome(parent)

Capillary disease(parent)

Leukoencephalopathy(parent)

Hereditary nephropathy(parent)

Renal vascular disorder(parent)

Changes in retinal vascular appearance(parent)

Chronic disorder of genitourinary system(parent)

Chronic disease of immune function(parent)

Type I interferonopathy(parent)

Chronic disease of immune structure(parent)

Genetic disease of glomerulus(parent)

Quick Facts

SNOMED CT: 783787000
UMLS CUI: C1860518
Fully Specified Name: Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations (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.