Intellectual disability, autosomal recessive 59

rare

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the IMPA1 gene.

Identifiers: MONDO:0015020 OMIM:617323
Causal genes: IMPA1
Part of: Autosomal recessive non-syndromic intellectual disability
Also known as: autosomal recessive non-syndromic intellectual disability caused by mutation in IMPA1 · IMPA1 autosomal recessive non-syndromic intellectual disability · intellectual disability, autosomal recessive type 59 · mental retardation, autosomal recessive 59 · mental retardation, autosomal recessive type 59

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