loading...| Preferred Name |
X-Linked Combined Immunodeficiency Diseases [Disease/Finding] |
|
| Synonyms |
Combined Immunodeficiency, X-Linked Immunodeficiency Diseases, X-Linked Combined Immunodeficiency 6 Severe Combined Immunodeficiency, X-Linked, T Cell-Negative, B Cell-Positive, NK Cell-Negative X-Linked SCID XSCID SCIDX1 X-Linked Immunodeficiency Disease X-Linked Combined Immunodeficiency Severe Combined Immunodeficiency, X-Linked Immunodeficiency 4 SCIDX X-Linked Combined Immunodeficiency Diseases SCID, X-Linked X-Linked Immunodeficiency Syndrome X-SCID X-Linked Severe Combined Immunodeficiency Severe Combined Immunodeficiency, X-Linked, T Cell Negative, B Cell Positive, NK Cell Negative |
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| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000181205 |
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| altLabel |
Combined Immunodeficiency, X-Linked Immunodeficiency Diseases, X-Linked Combined Immunodeficiency 6 Severe Combined Immunodeficiency, X-Linked, T Cell-Negative, B Cell-Positive, NK Cell-Negative X-Linked SCID XSCID SCIDX1 X-Linked Immunodeficiency Disease X-Linked Combined Immunodeficiency Severe Combined Immunodeficiency, X-Linked Immunodeficiency 4 SCIDX X-Linked Combined Immunodeficiency Diseases SCID, X-Linked X-Linked Immunodeficiency Syndrome X-SCID X-Linked Severe Combined Immunodeficiency Severe Combined Immunodeficiency, X-Linked, T Cell Negative, B Cell Positive, NK Cell Negative |
|
| cui |
C1279481 |
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| MESH DEFINITION |
Forms of combined immunodeficiency caused by mutations in the gene for INTERLEUKIN RECEPTOR COMMON GAMMA SUBUNIT. Both severe and non-severe subtypes of the disease have been identified. |
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| MESH DUI |
D053632 |
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| MeSH name |
X-Linked Combined Immunodeficiency Diseases |
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| MESH UI |
M0495084 |
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| NDFRT kind |
DISEASE_KIND |
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| notation |
N0000181205 |
|
| NUI |
N0000181205 |
|
| prefLabel |
X-Linked Combined Immunodeficiency Diseases [Disease/Finding] |
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| tui |
T047 |
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| subClassOf |