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Summary Literature (0)
OMIM:614257 - CHROMOSOME 20q11-q12 DELETION SYNDROME


Xenbase Genes: epb41l1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013658 - intellectual disability, autosomal dominant 11
MONDO:0100172 - intellectual disability, autosomal dominant

Disease Ontology (DO):
DOID:0070041 - autosomal dominant non-syndromic intellectual disability 11