8 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:2115 | B cell deficiency | A primary immunnodeficiency disease that is caused by a lack of infection-fighting antibody producing B cells (immunoglobulins) or B cells that are not functioning properly. |
| DOID:0080544 | hyper IgM syndrome | A hyperimmunoglobin syndrome that is characterized by an immune system that fails to produce normal levels of the antibodies IgA, IgG and IgE but can produce normal or elevated levels of IgM. |
| DOID:2959 | hyperimmunoglobulin syndrome | A B cell deficiency that is characterized by relative predominance of certain immunoglobulin subtypes and deficiencies of others. |
| DOID:0060760 | immunodeficiency with hyper-IgM type 4 | A hyper IgM syndrome that is characterized by normal or increased serum IgM concentrations associated with low or absent serum IgG, IgA, and IgE concentrations, indicating a defect in the class-switch recombination (CSR) process. |
7 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0080544 | DOID:0060760 |
| is_a | DOID:7 | DOID:0060760 |
| is_a | DOID:2914 | DOID:0060760 |
| is_a | DOID:4 | DOID:0060760 |
| is_a | DOID:2959 | DOID:0060760 |
| is_a | DOID:2115 | DOID:0060760 |
| is_a | DOID:612 | DOID:0060760 |
