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General Information
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| Term |
complement component 5 deficiency |
ID (Ontology) |
DOID:8158 (Human Disease) |
| Definition |
A complement deficiency that is characterized by susceptibility to recurrent bacterial infections especially to infections of enveloped organisms, and has_material_basis_in mutation in the complement component 5 (C5) gene on chromosome 9q33.2 that encodes the fifth component of complenent, a part of the innate immune system. |
| Also Known As |
"C5 deficiency" |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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complement component 5 deficiency | 3 | for disease ribbon | complement component 5 deficiency | 3 | model of | complement component 5 deficiency | 3 |
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