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Summary Literature (0)
MIM:609741 - CATARACT 22, MULTIPLE TYPES; CTRCT22

Xenbase Genes: crybb3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011060 - early-onset non-syndromic cataract
MONDO:0012336 - perianal skin

Disease Ontology (DO):
DOID:0110268 - cataract 22 multiple types