Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Domain and all descendants
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Choroideremia An X chromosome-linked abnormality characterized by atrophy of the choroid and degeneration of the retinal pigment epithelium causing night blindness. | Congenital Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110046 |
| Choroiditis Inflammation of the choroid. | Inflammatory Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110143 |
| Coloboma Congenital anomaly in which some of the structures of the eye are absent due to incomplete fusion of the fetal intraocular fissure during gestation. | Congenital Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110033 |
| Cone Dystrophy A general term which describes a group of rare eye disorders that affect the cone cells of the RETINA. Cone dystrophy can cause a variety of symptoms… | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110047 |
| Cone-Rod Dystrophies Genetically heterogeneous and sometimes syndromic (e.g., BARDET BIEDL SYNDROME; and SPINOCEREBELLAR ATAXIA TYPE 7) retinopathies with initial RETINAL… | Congenital Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110048 |
| Conjunctival Diseases Diseases involving the CONJUNCTIVA. | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110003 |
| Conjunctivitis INFLAMMATION of the CONJUNCTIVA. | Inflammatory Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110004 |
| Conjunctivitis, Allergic Conjunctivitis due to hypersensitivity to various allergens. | Immune Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110005 |
| Corneal Diseases Diseases of the cornea. | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110012 |
| Corneal Dystrophies, Hereditary Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescenc… | Congenital Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110013 |
| Corneal Dystrophy, Juvenile Epithelial of Meesmann An autosomal dominant form of hereditary corneal dystrophy due to a defect in cornea-specific KERATIN formation. Mutations in the genes that encode K… | Congenital Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110014 |
| Corneal Edema An excessive amount of fluid in the cornea due to damage of the epithelium or endothelium causing decreased visual acuity. | Pathologic Condition | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110016 |
| Corneal Endothelial Cell Loss Loss of CORNEAL ENDOTHELIUM usually following intraocular surgery (e.g., cataract surgery) or due to FUCHS' ENDOTHELIAL DYSTROPHY; ANGLE-CLOSURE GLAU… | Pathologic Condition | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110017 |
| Corneal Neovascularization New blood vessels originating from the corneal blood vessels and extending from the limbus into the adjacent CORNEAL STROMA. Neovascularization in th… | Vascular Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110018 |
| Corneal Opacity Disorder occurring in the central or peripheral area of the cornea. The usual degree of transparency becomes relatively opaque. | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110019 |
| Corneal Wavefront Aberration Asymmetries in the topography and refractive index of the corneal surface that affect visual acuity. | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110021 |
| Cyclodialysis Clefts Finding of a separation of the CILIARY BODY in the SCLERAL SPUR region, creating aqueous outflow from the ANTERIOR CHAMBER into suprachoroidal space … | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110031 |
| Dacryocystitis Inflammation of the lacrimal sac. (Dorland, 27th ed) | Inflammatory Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110075 |
| Diabetic Retinopathy Disease of the RETINA as a complication of DIABETES MELLITUS. It is characterized by the progressive microvascular complications, such as ANEURYSM, i… | Metabolic Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110112 |
| Dry Eye Syndromes Corneal and conjunctival dryness due to deficient tear production, predominantly in menopausal and post-menopausal women. Filamentary keratitis or er… | Syndrome | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110077 |
| Ectopia Lentis Congenital displacement of the lens resulting from defective zonule formation. | Congenital Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110034 |
| Ectropion The turning outward (eversion) of the edge of the eyelid, resulting in the exposure of the palpebral conjunctiva. (Dorland, 27th ed) | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110070 |
| Enophthalmos Recession of the eyeball into the orbit. | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110094 |
| Entropion The turning inward (inversion) of the edge of the eyelid, with the tarsal cartilage turned inward toward the eyeball. (Dorland, 27th ed) | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110071 |
| Epiretinal Membrane A membrane on the vitreal surface of the retina resulting from the proliferation of one or more of three retinal elements: (1) fibrous astrocytes; (2… | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110113 |
| Exfoliation Syndrome The deposition of flaky, translucent fibrillar material most conspicuous on the anterior lens capsule and pupillary margin but also in both surfaces … | Syndrome | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110147 |
| Exophthalmos Abnormal protrusion of both eyes; may be caused by endocrine gland malfunction, malignancy, injury, or paralysis of the extrinsic muscles of the eye. | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110095 |
| Eye Abnormalities Congenital absence of or defects in structures of the eye; may also be hereditary. | Congenital Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110026 |
| Eye Diseases Diseases affecting the eye. | Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110001 |
| Eye Diseases, Hereditary Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the ey… | Congenital Disorder | Pathology | Ophthalmology [curated_secondary] | AMW:DIS:110040 |