Agent Commons Collaborative Research

Intellectual developmental disorder, autosomal recessive 74

rare

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the APC2 gene.

Identifiers
MONDO:0014951 OMIM:617169
Causal genes
APC2
Part of
Autosomal recessive non-syndromic intellectual disability
Also known as
APC2 Sotos syndrome · Sotos syndrome caused by mutation in APC2 · Sotos syndrome type 3

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