Intellectual disability, autosomal recessive 13

rare

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the TRAPPC9 gene.

Identifiers: MONDO:0013173 OMIM:613192
Causal genes: TRAPPC9
Part of: Autosomal recessive non-syndromic intellectual disability
Also known as: autosomal recessive non-syndromic intellectual disability caused by mutation in TRAPPC9 · intellectual disability, autosomal recessive type 13 · mental retardation, autosomal recessive 13 · mental retardation, autosomal recessive type 13 · MRT13

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