1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0080807 | autosomal dominant craniodiaphyseal dysplasia | A craniodiaphyseal dysplasia that has_material_basis_in heterozygous mutation in the SOST gene on chromosome 17q21. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:4254 | osteosclerosis | A bone remodeling disease that results_in abnormal elevated bone density or mass. |