Retinal nerve fiber layer disorder
diseaseOn this page
Also known as disease of nerve fiber layer of retinadisease of nerve fibre layer of retinadisease or disorder of nerve fiber layer of retinadisease or disorder of nerve fibre layer of retinadisorder of nerve fiber layer of retinadisorder of nerve fibre layer of retinanerve fiber layer of retina diseasenerve fiber layer of retina disease or disordernerve fibre bundle defectnerve fibre layer of retina diseasenerve fibre layer of retina disease or disorderretinal nerve fiber bundle defectsretinal nerve fibre bundle defectsretinal nerve fibre bundle deficiency
Summary
Retinal nerve fiber layer disorder (MONDO:0003579) is a disease. A subtype of visual pathway disorder — 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 | retinal nerve fiber layer disorder |
| Mondo ID | MONDO:0003579 |
| DOID | DOID:5678 |
| SNOMED CT | 193428001 |
| UMLS | C3665426 |
| MedGen | 784046 |
| Anatomy (UBERON) | UBERON:0001793 |
| Is cancer (heuristic) | no |
Also known as: disease of nerve fiber layer of retina · disease of nerve fibre layer of retina · disease or disorder of nerve fiber layer of retina · disease or disorder of nerve fibre layer of retina · disorder of nerve fiber layer of retina · disorder of nerve fibre layer of retina · nerve fiber layer of retina disease · nerve fiber layer of retina disease or disorder · nerve fibre bundle defect · nerve fibre layer of retina disease · nerve fibre layer of retina disease or disorder · retinal nerve fiber bundle defects · retinal nerve fibre bundle defects · retinal nerve fibre bundle deficiency
Disease family
This is a subtype of visual pathway disorder. 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 body system or component › nervous system disorder › central nervous system disorder › brain disorder › visual pathway disorder › retinal nerve fiber layer disorder
Related subtypes (4): visual cortex disorder, coloboma of optic nerve, optic pathway glioma, optic tract meningioma
Subtypes (1): neuroretinitis
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.