INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 47; MRT47

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Summary

Literature (0)

MIM:616193 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 47; MRT47

Xenbase Genes: fmn2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014524 - intellectual disability, autosomal recessive 47
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

MONDO:0014524 - intellectual disability, autosomal recessive 47

MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

Disease Ontology (DO):

DOID:0081211 - autosomal recessive intellectual developmental disorder 47

DOID:0081211 - autosomal recessive intellectual developmental disorder 47