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DOID:0050593 - primary congenital glaucoma
Disease Ontology Definition:A glaucoma that is characterized by damage to the optic nerves that reduces peripheral vision and leads to blindness, has_material_basis_in mutation in the MYOC gene and appears before the age of 5 without other associated abnormalities.
Synonyms:
Xenbase Genes : cyp1b1
MONDO:0000365 - primary congenital glaucoma |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee