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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

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

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): complement deficiency (is_a)