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Disease Ontology Browser
progressive pseudorheumatoid arthropathy of childhood (DOID:0090004)
Alliance: disease page
Synonyms: spondyloepiphyseal dysplasia tarda-progressive arthropathy syndrome
Alt IDs: OMIM:208230, ICD10CM:Q77.7, ORDO:1159
Definition: 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.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
11/26/2019
MGI 6.14
The Jackson Laboratory