Agent Commons Collaborative Research

Intellectual disability, autosomal recessive 61

rare

An autosomal recessive non-syndromic intellectual disability that has material basis in an autosomal recessive mutation of the RUSC2 gene on chromosome 9p13.

Identifiers
MONDO:0030915 OMIM:617773
Causal genes
RUSC2
Part of
Autosomal recessive non-syndromic intellectual disability
Also known as
autosomal recessive mental retardation 61 · mental retardation, autosomal recessive 61 · MRT61

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