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About:
primary congenital glaucoma
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An Entity of Type :
owl:Class
, within Data Space :
linkeddata.uriburner.com:28898
associated with source
document(s)
New Facet based on Instances of this Class
Xref MGI.
Attributes
Values
type
Class
subClassOf
monogenic disease
physical disorder
glaucoma
nodeID://b50937182
nodeID://b50937183
label
primary congenital glaucoma
comment
Xref MGI.
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0050593
database_cross_reference
OMIM:613085
OMIM:613086
has_obo_namespace
disease_ontology
http://purl.obolib...g/obo/IAO_0000115
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.
is
subClassOf
of
hydrophthalmos
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50937184
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