Term Name:	X-linked properdin deficiency
Synonyms:	CFPD, complement factor properdin deficiency
Definition:	A complement deficiency characterized by decreased plasma levels of complement factor properdin and increased susceptibility to Neisseria species infections that has_material_basis_in homozygous or hemizygous mutation in PFC on chromosome Xp11.23.
Ontology:	Human Disease [DOID:0111768]   ( DOID:0111768 )