Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Any direct membership
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Uveal Diseases Diseases of the uvea. | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110139 |
| Uveal Effusion Syndrome Rare disease characterized by suprachoroidal fluid accumulation between the CHOROID and the SCLERA, annular detachment of the CHOROID, often with sec… | Syndrome | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110032 |
| Uveitis Inflammation of part or all of the uvea, the middle (vascular) tunic of the eye, and commonly involving the other tunics (sclera and cornea, and the … | Inflammatory Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110150 |
| Uveitis, Anterior Inflammation of the anterior uvea comprising the iris, angle structures, and the ciliary body. Manifestations of this disorder include ciliary inject… | Inflammatory Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110153 |
| Uveitis, Intermediate Inflammation of the pars plana, ciliary body, and adjacent structures. | Inflammatory Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110156 |
| Uveitis, Posterior Inflammation of the choroid as well as the retina and vitreous body. Some form of visual disturbance is usually present. The most important character… | Inflammatory Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110154 |
| Vitelliform Macular Dystrophy Autosomal dominant hereditary maculopathy with childhood-onset accumulation of LIPOFUSION in RETINAL PIGMENT EPITHELIUM. Affected individuals develop… | Congenital Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110120 |
| Vitreoretinopathy, Proliferative Vitreoretinal membrane shrinkage or contraction secondary to the proliferation of primarily retinal pigment epithelial cells and glial cells, particu… | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110136 |
| Vitreous Detachment Detachment of the corpus vitreum (VITREOUS BODY) from its normal attachments, especially the retina, due to shrinkage from degenerative or inflammato… | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110158 |
| Vitreous Hemorrhage Hemorrhage into the VITREOUS BODY. | Vascular Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110059 |
| Weill-Marchesani Syndrome Rare congenital disorder of connective tissue characterized by brachydactyly, joint stiffness, childhood onset of ocular abnormalities (e.g., microsp… | Syndrome | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:050014 |
| Wet Macular Degeneration The label is process-shaped, but the organ-specific concept may also function as a disorder; manual semantic review is required. | Pathological process | Pathology | Ophthalmology [curated_secondary] | AMW:PROC:135081 |
| White Dot Syndromes A group of idiopathic multifocal posterior uveitis syndromes involving the CHOROID; RETINAL PIGMENT EPITHELIUM; and RETINA. They are characterized by… | Syndrome | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110155 |
| Xerophthalmia Dryness of the eye surfaces caused by deficiency of tears or conjunctival secretions. It may be associated with vitamin A deficiency, trauma, or any … | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110011 |