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Browse canonical concepts by label, domain, node type, prefix and encoded class.

164 results

Current membership scope: Domain and all descendants

ConceptNode typeBase domainMatched membershipIdentifier
Choroideremia
An X chromosome-linked abnormality characterized by atrophy of the choroid and degeneration of the retinal pigment epithelium causing night blindness.
Congenital DisorderPathologyOphthalmology [curated_secondary]AMW:DIS:110046
Choroiditis
Inflammation of the choroid.
Inflammatory DisorderPathologyOphthalmology [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 DisorderPathologyOphthalmology [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…
DisorderPathologyOphthalmology [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 DisorderPathologyOphthalmology [curated_secondary]AMW:DIS:110048
Conjunctival Diseases
Diseases involving the CONJUNCTIVA.
DisorderPathologyOphthalmology [curated_secondary]AMW:DIS:110003
Conjunctivitis
INFLAMMATION of the CONJUNCTIVA.
Inflammatory DisorderPathologyOphthalmology [curated_secondary]AMW:DIS:110004
Conjunctivitis, Allergic
Conjunctivitis due to hypersensitivity to various allergens.
Immune DisorderPathologyOphthalmology [curated_secondary]AMW:DIS:110005
Corneal Diseases
Diseases of the cornea.
DisorderPathologyOphthalmology [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 DisorderPathologyOphthalmology [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 DisorderPathologyOphthalmology [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 ConditionPathologyOphthalmology [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 ConditionPathologyOphthalmology [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 DisorderPathologyOphthalmology [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.
DisorderPathologyOphthalmology [curated_secondary]AMW:DIS:110019
Corneal Wavefront Aberration
Asymmetries in the topography and refractive index of the corneal surface that affect visual acuity.
DisorderPathologyOphthalmology [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 …
DisorderPathologyOphthalmology [curated_secondary]AMW:DIS:110031
Dacryocystitis
Inflammation of the lacrimal sac. (Dorland, 27th ed)
Inflammatory DisorderPathologyOphthalmology [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 DisorderPathologyOphthalmology [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…
SyndromePathologyOphthalmology [curated_secondary]AMW:DIS:110077
Ectopia Lentis
Congenital displacement of the lens resulting from defective zonule formation.
Congenital DisorderPathologyOphthalmology [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)
DisorderPathologyOphthalmology [curated_secondary]AMW:DIS:110070
Enophthalmos
Recession of the eyeball into the orbit.
DisorderPathologyOphthalmology [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)
DisorderPathologyOphthalmology [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…
DisorderPathologyOphthalmology [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 …
SyndromePathologyOphthalmology [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.
DisorderPathologyOphthalmology [curated_secondary]AMW:DIS:110095
Eye Abnormalities
Congenital absence of or defects in structures of the eye; may also be hereditary.
Congenital DisorderPathologyOphthalmology [curated_secondary]AMW:DIS:110026
Eye Diseases
Diseases affecting the eye.
DisorderPathologyOphthalmology [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 DisorderPathologyOphthalmology [curated_secondary]AMW:DIS:110040