1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0080044 | hypochondrogenesis | An osteochondrodysplasia that has_material_basis_in a mutation in the COL2A1 gene which affects bone growth and results_in a small body, hydrops fetalis, and abnormal ossification located_in vertebral column or located_in pelvis. The disease has_symptom enlarged abdomen. |
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. |
