1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0070300 | multiple epiphyseal dysplasia 4 | A multiple epiphyseal dysplasia that has_material_basis_in homozygous mutation in the SLC26A2 gene on chromosome 5q32. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:2256 | osteochondrodysplasia | A bone development disease that results_in defective development of cartilage or bone. |