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| Term | complement component 3 deficiency | ID (Ontology) | DOID:8354 (Human Disease) |
| Definition | A complement deficiency that is characterized by deficiency of complement component 3 that increases susceptibility to infection and autoimmune diseases and has_material_basis_in autosomal recessive inheritance of mutation in the C3 gene on chromosome 19p13.3, has_symptom recurrent bacterial infections. | ||
| Also Known As | "C3 deficiency" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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primary immunodeficiency disease |__complement deficiency |__complement component 3 deficiency 3 rec. |
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| Is a | complement deficiency | ||
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External Crossreferences & Linkouts
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MIM:613779 NCI:C9468 ORDO:280133 SNOMEDCT_US_2023_03_01:771443008 UMLS_CUI:C1332655 |
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