INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 13; MRT13

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)

MIM:613192 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 13; MRT13

Xenbase Genes: trappc9

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013173 - intellectual disability, autosomal recessive 13
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

MONDO:0013173 - intellectual disability, autosomal recessive 13

MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

Disease Ontology (DO):

DOID:0050889 - non-syndromic intellectual disability
DOID:0081098 - autosomal recessive intellectual developmental disorder 13

DOID:0050889 - non-syndromic intellectual disability

DOID:0081098 - autosomal recessive intellectual developmental disorder 13