Central visual impairment

disorder

SNOMED 432141000124105CUI C3810365

Overview

Central visual impairment 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 the cerebral white matter

Frequent (30-79%)HP:0002500

Brain imaging abnormality

Frequent (30-79%)HP:0410263

Frequent (30-79%)HP:0100021

Dull intelligence

Frequent (30-79%)HP:0001249

Impaired visuospatial constructive cognition

Frequent (30-79%)HP:0010794

Premature birth

Frequent (30-79%)HP:0001622

Abnormal brain morphology

Occasional (5-29%)HP:0012443

Abnormal cerebral morphology

Occasional (5-29%)HP:0002060

Abnormal visual accommodation

Occasional (5-29%)HP:0030800

Abnormal visual pursuit

Occasional (5-29%)HP:0007772

Abnormality of refraction

Occasional (5-29%)HP:0000539

ASD

Occasional (5-29%)HP:0000729

Brain inflammation

Occasional (5-29%)HP:0002383

Central nervous system degeneration

Occasional (5-29%)HP:0007009

Central nervous system infection

Occasional (5-29%)HP:0011450

Childhood attention deficit/hyperactivity disorder

Occasional (5-29%)HP:0007018

Clumsiness

Occasional (5-29%)HP:0002312

Decreased size of cranium

Occasional (5-29%)HP:0000252

Defective or absent horizontal voluntary eye movements

Occasional (5-29%)HP:0000657

Dysmetric eye movements

Occasional (5-29%)HP:0000641

Epilepsy

Occasional (5-29%)HP:0001250

Eye movement issue

Occasional (5-29%)HP:0000496

Focal cortical dysplasia

Occasional (5-29%)HP:0032046

Hypoplastic optic nerves

Occasional (5-29%)HP:0000609

Increased cup-to-disc ratio

Occasional (5-29%)HP:0012796

Intracranial haemorrhage

Occasional (5-29%)HP:0002170

Involuntary, rapid, rhythmic eye movements

Occasional (5-29%)HP:0000639

Ischemic stroke

Occasional (5-29%)HP:0002140

Meningitis

Occasional (5-29%)HP:0001287

Neonatal hypoglycemia

Occasional (5-29%)HP:0001998

Related Conditions

Cortical visual impairment(parent)

Quick Facts

SNOMED CT: 432141000124105
UMLS CUI: C3810365
Fully Specified Name: Central visual impairment (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.