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Summary Literature (0)
OMIM:615502 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21


Xenbase Genes: ctcf

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014213 - intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome

Disease Ontology (DO):
DOID:0070051 - autosomal dominant non-syndromic intellectual disability 21