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Summary Literature (0)
OMIM:611092 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 6; MRT6


Xenbase Genes: grik2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012614 - intellectual disability, autosomal recessive 6
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

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