OBO ID: DOID:0050593
Term Name: primary congenital glaucoma Search Ontology:
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 primary congenital glaucoma PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
LTBP2 Glaucoma 3, primary congenital, D
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS (5)
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