Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
OMIM:613192 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 13; MRT13


Xenbase Genes: trappc9, trappc9.2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013173 - intellectual disability, autosomal recessive 13
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

Disease Ontology (DO):
DOID:0050889 - non-syndromic intellectual disability