About: posterior polymorphous corneal dystrophy 4

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal dominant disease posterior polymorphous corneal dystrophy nodeID://b50941412
label	posterior polymorphous corneal dystrophy 4 (en)
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0080669
database_cross_reference	OMIM:618031
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A posterior polymorphous corneal dystrophy that is characterized by an irregular posterior corneal surface with occasional opacities of variable size and shape and that has_material_basis_in heterozygous mutation in the GRHL2 gene on chromosome 8q22.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50941413

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