Agent Commons Collaborative Research
Hereditary glaucoma
rareHereditary glaucoma is a clinically diverse group of rare eye disorders with genetic predisposition characterized by elevated intraocular pressure (IOP) and glaucomatous changes of the optic nerve head, leading to field defects, visual loss and blindness. Hereditary glaucoma can be sub-classified as primary (congenital glaucoma, juvenile glaucoma) or secondary according to the presence or absence of systemic or other ocular anomalies (iridogoniodysgenesis, Stickler syndrome, Coats syndrome). The clinical presentation is variable and is based on age, severity of glaucoma, presence of ocular abnormalities and development of secondary IOP related abnormalities.
- Identifiers
- MONDO:0018174 Orphanet:359
- Part of
- GlaucomaHereditary disease
- Also known as
- glaucoma, hereditary · hereditary glaucoma (disease)
Subtypes
Disease Rare Not rare Subtypes
- Congenital glaucoma MONDO:0020366 9
- Juvenile open angle glaucoma MONDO:0020367 6
- TEK-related primary glaucoma MONDO:0800182 1
- OPTN-related open angle glaucoma MONDO:0100553 OPTN
- Anterior segment dysgenesis 3 MONDO:0024456
- Glaucoma 1, open angle, O MONDO:0013134 NTF4
- Glaucoma 1, open angle, P MONDO:0008328
- Glaucoma secondary to spherophakia/ectopia lentis and megalocornea MONDO:0016559
- Hereditary glaucoma, primary closed-angle MONDO:0030038 COL18A1
- Iris hypoplasia with glaucoma MONDO:0010633
Projects
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