Intellectual disability, autosomal recessive 13

MONDO:0013173

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

Also known as: TRAPPC9 autosomal recessive non-syndromic intellectual disability, autosomal recessive non-syndromic intellectual disability caused by mutation in TRAPPC9, intellectual disability, autosomal recessive 13, intellectual disability, autosomal recessive type 13, mental retardation, autosomal recessive type 13, MRT13, mental retardation, autosomal recessive 13

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, autosomal recessive 13 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal recessive non-syndromic intellectual disability (0)

Including sub-types (0) Tagged with Intellectual disability, autosomal recessive 13 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.