Human genes for primary congenital glaucoma
Primary congenital glaucoma [DOID:0050593]
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: primary congenital glaucoma, DOID:0050593, primary congenital glaucomas