1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111161 | Crouzon syndrome-acanthosis nigricans syndrome | A syndrome characterized by Crouzon-like features, premature synostosis of cranial sutures, and acanthosis nigricans that has_material_basis_in heterozygous missense mutation in the FGFR3 gene on chromosome 4p16. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:65 | connective tissue disease | A musculoskeletal system disease that affects tissues such as skin, tendons, and cartilage. |
