CHROMOSOME 20q11-q12 DELETION SYNDROME

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:614257 - CHROMOSOME 20q11-q12 DELETION SYNDROME

Xenbase Genes: epb41l1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013658 - intellectual disability, autosomal dominant 11
MONDO:0100172 - intellectual disability, autosomal dominant

MONDO:0013658 - intellectual disability, autosomal dominant 11

MONDO:0100172 - intellectual disability, autosomal dominant

Disease Ontology (DO):

DOID:0070041 - autosomal dominant intellectual developmental disorder 11

DOID:0070041 - autosomal dominant intellectual developmental disorder 11