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loading...| Preferred Name |
Wiskott-Aldrich Syndrome [Disease/Finding] |
|
| Synonyms |
Wiskott Syndrome |
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| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000003164 |
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| altLabel |
Wiskott Syndrome Eczema-Thrombocytopenia-Immunodeficiency Syndrome Imd2 Immunodeficiency 2 Aldrich Syndrome Wiskott-Aldrich Syndrome |
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| cui |
C0043194 |
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| MESH DEFINITION |
A rare, X-linked immunodeficiency syndrome characterized by ECZEMA; LYMPHOPENIA; and, recurrent pyogenic infection. It is seen exclusively in young boys. Typically, IMMUNOGLOBULIN M levels are low and IMMUNOGLOBULIN A and IMMUNOGLOBULIN E levels are elevated. Lymphoreticular malignancies are common. |
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| MESH DUI |
D014923 |
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| MeSH name |
Wiskott-Aldrich Syndrome |
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| MESH UI |
M0022985 |
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| NDFRT kind |
DISEASE_KIND |
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| notation |
N0000003164 |
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| NUI |
N0000003164 |
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| prefLabel |
Wiskott-Aldrich Syndrome [Disease/Finding] |
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| SNOMED CID |
36070007 |
|
| tui |
T047 |
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| subClassOf |
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