INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21

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Summary

Literature (0)

MIM: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

MONDO:0014213 - intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome

Disease Ontology (DO):

DOID:0070051 - autosomal dominant intellectual developmental disorder 21

DOID:0070051 - autosomal dominant intellectual developmental disorder 21