Intellectual disability, autosomal recessive 47

rare

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the FMN2 gene.

Identifiers: MONDO:0014524 OMIM:616193
Causal genes: FMN2
Part of: Autosomal recessive non-syndromic intellectual disability
Also known as: autosomal recessive non-syndromic intellectual disability caused by mutation in FMN2 · FMN2 autosomal recessive non-syndromic intellectual disability · intellectual developmental disorder, autosomal recessive 47 · intellectual disability, autosomal recessive type 47 · mental retardation, autosomal recessive 47

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