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:0111965 | T cell, B cell, and NK cell deficiency | A combined immunodeficiency characterized by impaired function or reduced numbers of T cells, B cells, and natural killer (NK) cells. |
10 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:0111965 | DOID:0061079 |
is_a | DOID:0111965 | DOID:0061085 |
is_a | DOID:0111965 | DOID:0061088 |
is_a | DOID:0111965 | DOID:0061093 |
is_a | DOID:0111962 | DOID:0111965 |
is_a | DOID:7 | DOID:0111965 |
is_a | DOID:2914 | DOID:0111965 |
is_a | DOID:4 | DOID:0111965 |
is_a | DOID:612 | DOID:0111965 |
is_a | DOID:0111965 | DOID:0111980 |