MCID: PHC002
MIFTS: 25
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Phacogenic Glaucoma
Categories:
Eye diseases, Neuronal diseases
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MalaCards integrated aliases for Phacogenic Glaucoma:Classifications:External Ids:
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Disease Ontology :
12
A glaucoma characterized by glaucomatous optic atrophy secondary to a lens abnormality and has symptom progressive decreased vision, especially decreased peripheral vision. Phacogenic glaucoma can be caused by cataracts, trauma to the eye, or age-related damage that obstructs aqueous outflow, leading to inappropriately increased intraocular pressure and eventual optic nerve atrophy with associated vision loss.
MalaCards based summary : Phacogenic Glaucoma is related to exfoliation syndrome and phacolytic glaucoma, and has symptoms including progressive decreased vision An important gene associated with Phacogenic Glaucoma is LOXL1 (Lysyl Oxidase Like 1), and among its related pathways/superpathways are Phospholipase-C Pathway and Degradation of the extracellular matrix. Affiliated tissues include eye, and related phenotype is respiratory system. |
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MalaCards organs/tissues related to Phacogenic Glaucoma:40
Eye
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Articles related to Phacogenic Glaucoma:
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Search
GEO
for disease gene expression data for Phacogenic Glaucoma.
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Pathways related to Phacogenic Glaucoma according to GeneCards Suite gene sharing:
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Cellular components related to Phacogenic Glaucoma according to GeneCards Suite gene sharing:
Biological processes related to Phacogenic Glaucoma according to GeneCards Suite gene sharing:
Molecular functions related to Phacogenic Glaucoma according to GeneCards Suite gene sharing:
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