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Summary Literature (0)
OMIM:312060 - PROPERDIN DEFICIENCY, X-LINKED; CFPD


Xenbase Genes: cfp

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010713 - properdin deficiency, X-linked

Disease Ontology (DO):
DOID:0111768 - X-linked properdin deficiency