Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Agenesis of corpus callosum
Occasional (5-29%)
Glutamate-cysteine ligase deficiency
Occasional (5-29%)
Childhood absence epilepsy
Occasional (5-29%)
Rheumatic fever
Occasional (5-29%)
Sarcosine dehydrogenase deficiency
Occasional (5-29%)
Acute rheumatic arthritis
Occasional (5-29%)
Acute rheumatic fever
Occasional (5-29%)
Semantic dementia
Frequent (30-79%)
Marchiafava-Bignami disease
Occasional (5-29%)
Congenital bilateral perisylvian syndrome
Stormorken syndrome
Benson syndrome
Frequent (30-79%)
Primary progressive non fluent aphasia
Frequent (30-79%)
Behavioral variant of frontotemporal dementia
Very frequent (80-99%)
Autosomal dominant optic atrophy and cataract
Occasional (5-29%)
Adult-onset dystonia parkinsonism
Frequent (30-79%)
Bilateral polymicrogyria
Frequent (30-79%)
Monosomy 15q11.2
Frequent (30-79%)
Atypical progressive supranuclear palsy syndrome
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 9236007
- UMLS CUI
- C0002018
- Fully Specified Name
- Alexia (finding)
- Associated Conditions
- 19
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.