Search Ontology:
Human Disease
complement component 5 deficiency
- Term ID
- DOID:8158
- Synonyms
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- C5 deficiency
- 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. (2)
- References
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- MESH:C537005
- MIM:609536
- NCI:C9469
- ORDO:169150
- Ontology
- Human Disease ( DOID:8158 )
- is a type of
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Genes Involved
Zebrafish Models