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loading...| Preferred Name |
Bare Lymphocyte Syndrome |
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| Synonyms |
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| Definitions |
A hereditary immunodeficiency disorder caused by the lack of expression of major histocompatibility complex (MHC) proteins. Signs include upper and lower respiratory tract bacterial infections, malabsorption, diarrhea, and mucocutaneous candidiasis. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C3895 |
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| code |
C3895 |
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| definition |
A hereditary immunodeficiency disorder caused by the lack of expression of major histocompatibility complex (MHC) proteins. Signs include upper and lower respiratory tract bacterial infections, malabsorption, diarrhea, and mucocutaneous candidiasis. |
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| label |
Bare Lymphocyte Syndrome |
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| Legacy Concept Name |
Bare_Lymphocyte_Syndrome |
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| Preferred_Name |
Bare Lymphocyte Syndrome |
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| prefixIRI |
NCIT:C3895 |
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| prefLabel |
Bare Lymphocyte Syndrome |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0242583 |
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| subClassOf |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/RCD/X20HL | RCD | LOOM | |
| http://sbmi.uth.tmc.edu/ontology/ochv#24878 | OCHV | LOOM | |
| http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3895 | NCIT | LOOM | |
| http://sbmi.uth.tmc.edu/ontology/ochv#C0242583 | OCHV | LOOM |