Intellectual disability, autosomal recessive 51

rare

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

Identifiers: MONDO:0014759 OMIM:616739
Causal genes: HNMT
Part of: Autosomal recessive non-syndromic intellectual disability
Also known as: autosomal recessive non-syndromic intellectual disability caused by mutation in HNMT · HNMT autosomal recessive non-syndromic intellectual disability · intellectual developmental disorder, autosomal recessive 51 · intellectual disability, autosomal recessive type 51 · mental retardation, autosomal recessive 51

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