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Summary Literature (0)
MIM:616973 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 42; MRD42


Xenbase Genes: gnb1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014855 - intellectual disability, autosomal dominant 42

Disease Ontology (DO):
DOID:0070072 - autosomal dominant intellectual developmental disorder 42