1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0110881 | holoprosencephaly 1 | A holoprosencephaly that has_material_basis_in variation in the chromosome region 21q22.3. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:0080015 | physical disorder | A disease that has_material_basis_in a genetic abnormality, error with embryonic development, infection or compromised intrauterine environment. |