1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0111052 | Scott syndrome | A blood coagulation disease characterized by autosomal recessive inheritance of hemorrhagic episodes due to impaired platelet coagulant activity that has_material_basis_in homozygous mutation in the TMEM16F gene on chromosome 12q12. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:74 | hematopoietic system disease | A disease of anatomical entity that has_material_basis_in hematopoietic cells. |