Summary Literature (0)

DOID:8354 - complement component 3 deficiency

Disease 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.

Synonyms: C3 deficiency

Xenbase Genes : c3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013417 - complement component 3 deficiency

MIM:

MIM:613779 - COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE; C3D

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee