1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0110918 | hereditary spherocytosis type 3 | A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTA1 gene on chromosome 1q23.1. |
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. |
