Disease-gene associations mined from literature

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