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Summary Literature (0)
OMIM:614249 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 18, WITH OR WITHOUT EPILEPSY; MRT18


Xenbase Genes: med23

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013651 - intellectual disability, autosomal recessive 18
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

Disease Ontology (DO):
DOID:0060308 - autosomal recessive non-syndromic intellectual disability