Intellectual disability, autosomal recessive 51

MONDO:0014759

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

Also known as: HNMT autosomal recessive non-syndromic intellectual disability, MRT51, autosomal recessive non-syndromic intellectual disability caused by mutation in HNMT, intellectual developmental disorder, autosomal recessive 51, intellectual disability, autosomal recessive 51, intellectual disability, autosomal recessive type 51, mental retardation, autosomal recessive 51, mental retardation, autosomal recessive type 51

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