About: posterior amorphous corneal dystrophy

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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 chromosomal deletion syndrome stromal dystrophy nodeID://b50938866 nodeID://b50938871
label	posterior amorphous corneal dystrophy
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0060452
created_by	elvira
creation_date	2015-10-16T17:48:04Z
database_cross_reference	ICD10CM:H18.5 MESH:C567546 OMIM:612868 ORDO:98971
has_exact_synonym	PACD (en) chromosome 12q21.33 deletion syndrome
has_obo_namespace	disease_ontology
in_subset	DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115	A stromal dystrophy that is characterized by irregular sheetlike areas of opacification with involvement of the Descemet membrane and, in some instances, alterations of the normal endothelial mosaic and that has_material_basis_in a chromosome 12q21.33 contiguous gene deletion syndrome.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50938872

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