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Summary Literature (0)
DOID:0060295 - complement component 2 deficiency

Disease Ontology Definition:A complement deficiency that is characterized by recurrent bacterial infections, has_material_basis_in autosomal recessive inheritance of mutation in the C2 gene.

Synonyms:

Xenbase Genes : c2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009006 - complement component 2 deficiency

MIM:
MIM:217000 - COMPLEMENT COMPONENT 2 DEFICIENCY; C2D

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

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