Intellectual disability, autosomal recessive 52

MONDO:0014815

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the LMAN2L gene.

Also known as: LMAN2L autosomal recessive non-syndromic intellectual disability, MRT52, autosomal recessive non-syndromic intellectual disability caused by mutation in LMAN2L, intellectual developmental disorder, autosomal recessive 52, intellectual disability, autosomal recessive 52, intellectual disability, autosomal recessive type 52, mental retardation, autosomal recessive 52, mental retardation, autosomal recessive type 52

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↑ Autosomal recessive non-syndromic intellectual disability (0)

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