|OBO ID: DOID:8354|
|Term Name:||complement component 3 deficiency||Search Ontology:|
|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. https://www.omim.org/entry/613779|
|Ontology:||Human Disease (DOID:8354)|
|is a type of:||
OTHER complement component 3 deficiency PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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