9 Parents
Identifier | Name | Description |
---|---|---|
DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |
DOID:4 | disease | A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. |
DOID:0080015 | physical disorder | A disease that has_material_basis_in a genetic abnormality, error with embryonic development, infection or compromised intrauterine environment. |
DOID:74 | hematopoietic system disease | A disease of anatomical entity that has_material_basis_in hematopoietic cells. |
DOID:0050590 | severe congenital neutropenia | A neutropenia characterized by a maturation arrest of granulopoiesis at the level or promyelocytes and early onset of severe bacterial infections. |
DOID:1227 | neutropenia | |
DOID:12987 | agranulocytosis | A leukopenia that is characterized by a severe lack of of granulocytes with a drop in granulocyte concentration below 200 cells/mm³ of blood. |
DOID:9500 | leukocyte disease | A hematopoietic system disease that is located_in white blood cells. |
DOID:615 | leukopenia | A leukocyte disorder that is characterized by a decrease in the number of white blood cells (leukocytes) found in the blood, which places individuals at increased risk of infection. |
18 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:0080015 | DOID:0050590 |
is_a | DOID:1227 | DOID:0050590 |
is_a | DOID:74 | DOID:0050590 |
is_a | DOID:12987 | DOID:0050590 |
is_a | DOID:4 | DOID:0050590 |
is_a | DOID:9500 | DOID:0050590 |
is_a | DOID:615 | DOID:0050590 |
is_a | DOID:7 | DOID:0050590 |
is_a | DOID:0050590 | DOID:0080625 |
is_a | DOID:0050590 | DOID:0112128 |
is_a | DOID:0050590 | DOID:0112129 |
is_a | DOID:0050590 | DOID:0112130 |
is_a | DOID:0050590 | DOID:0112131 |
is_a | DOID:0050590 | DOID:0112132 |
is_a | DOID:0050590 | DOID:0112133 |
is_a | DOID:0050590 | DOID:0112134 |
is_a | DOID:0050590 | DOID:0112135 |
is_a | DOID:0050590 | DOID:0112136 |