6 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:2914 | immune system disease | A disease of anatomical entity that is located_in the immune system. |
DOID:612 | primary immunodeficiency disease | An immune system disease that results when one or more essential parts of the immune system is missing or not working properly at birth due to a genetic mutation. |
DOID:0111962 | combined immunodeficiency | A primary immunodeficiency disease that involves multiple components of the immune system. |
DOID:628 | combined T cell and B cell immunodeficiency | A primary immunodeficiency disease characterized by impaired T cell-mediated immunity and impaired B cell mediated humoral immunity. |
27 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:628 | DOID:0060021 |
is_a | DOID:628 | DOID:0060022 |
is_a | DOID:628 | DOID:0060028 |
is_a | DOID:628 | DOID:0080319 |
is_a | DOID:628 | DOID:0080492 |
is_a | DOID:628 | DOID:0110910 |
is_a | DOID:628 | DOID:0110912 |
is_a | DOID:628 | DOID:0111935 |
is_a | DOID:628 | DOID:0111936 |
is_a | DOID:628 | DOID:0111939 |
is_a | DOID:628 | DOID:0111948 |
is_a | DOID:628 | DOID:0111949 |
is_a | DOID:628 | DOID:0111951 |
is_a | DOID:628 | DOID:0111953 |
is_a | DOID:628 | DOID:0111954 |
is_a | DOID:628 | DOID:0111960 |
is_a | DOID:628 | DOID:0111982 |
is_a | DOID:628 | DOID:0111984 |
is_a | DOID:628 | DOID:0111992 |
is_a | DOID:628 | DOID:0112005 |
is_a | DOID:628 | DOID:5813 |
is_a | DOID:0111962 | DOID:628 |
is_a | DOID:2914 | DOID:628 |
is_a | DOID:612 | DOID:628 |
is_a | DOID:4 | DOID:628 |
is_a | DOID:7 | DOID:628 |
is_a | DOID:628 | DOID:6612 |