About: progressive pseudorheumatoid arthropathy of childhood

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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 recessive disease osteochondrodysplasia nodeID://b50942039 nodeID://b50942040
label	progressive pseudorheumatoid arthropathy of childhood
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0090004
database_cross_reference	ICD10CM:Q77.7 OMIM:208230 ORDO:1159
has_exact_synonym	spondyloepiphyseal dysplasia tarda-progressive arthropathy syndrome (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A osteochondrodysplasia characterized by autosomal recessive inheritance with typical onset around 3 years of age, progressive severe degenerative joint disease, platyspondyly, epiphyseal enlargement but absence of inflammatory joint disease that has_material_basis_in homozygous or compound heterozygous mutation in the CHST3 gene on chromosome 10q22.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50942041

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