1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0090004 | progressive pseudorheumatoid arthropathy of childhood | 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. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:17 | musculoskeletal system disease | A disease of anatomical entity that occurs in the muscular and/or skeletal system. |
