Human genes for complement component 3 deficiency
Complement component 3 deficiency [DOID:8354]
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.
Synonyms: complement component 3 deficiency, DOID:8354, C3 deficiency
Linkouts: OMIM