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Summary Literature (0)
MIM:604168 - CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN

Xenbase Genes: ctdp1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011402 - congenital cataracts-facial dysmorphism-neuropathy syndrome