Alexia without agraphia
diseaseOn this page
Also known as agnosia, visual verbalAgnosias, visual verbalagraphia, alexia withoutAgraphias, alexia withoutalexia syndrome without agraphiaalexia without Agraphiasalexias, Pureblindness, Pure WordBlindnesses, Pure WordPure alexiaPure alexia without agraphiaPure alexiasPure Word blindnessPure Word Blindnessesverbal agnosia, visualverbal Agnosias, visualvisual verbal agnosiavisual verbal Agnosiaswithout agraphia, alexia
Summary
Alexia without agraphia (MONDO:0000686) is a disease. A subtype of visual agnosia — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | alexia without agraphia |
| Mondo ID | MONDO:0000686 |
| MeSH | D020237 |
| DOID | DOID:0060156 |
| UMLS | C0751840 |
| MedGen | 155643 |
| GARD | 0027561 |
| Is cancer (heuristic) | no |
Also known as: agnosia, visual verbal · Agnosias, visual verbal · agraphia, alexia without · Agraphias, alexia without · alexia syndrome without agraphia · alexia without agraphia · alexia without Agraphias · alexias, Pure · blindness, Pure Word · Blindnesses, Pure Word · Pure alexia · Pure alexia without agraphia · Pure alexias · Pure Word blindness · Pure Word Blindnesses · verbal agnosia, visual · verbal Agnosias, visual · visual verbal agnosia · visual verbal Agnosias · without agraphia, alexia (+3 more)
Disease family
This is a subtype of visual agnosia. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease › human disease › disease by developmental or physiological process › psychiatric disorder › mental disorder › visual agnosia › alexia without agraphia
Related subtypes (6): apperceptive agnosia, associative visual agnosia, color agnosia, form agnosia, topographical agnosia, alexia
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 0.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.