Search Ontology:
Human Disease

primary congenital glaucoma

Term ID
DOID:0050593
Synonyms
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. https://ghr.nlm.nih.gov/condition/early-onset-glaucoma
References
Ontology
Human Disease   ( DOID:0050593 )
Relationships
is a type of
has subtype
Other Pages
Genes Involved
Zebrafish Models