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Summary Literature (0)
OMIM:616193 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 47; MRT47


Xenbase Genes: fmn2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014524 - intellectual disability, autosomal recessive 47
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability